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Concept IDs
SNOMEDCT
281300000
conceptId
281300000
fullName
Below reference range (qualifier value)
preferred
Below reference range (qualifier value)
Below reference range
preferredName
Below reference range
semanticTag
qualifier value
synonym
Below reference range
description
Below reference range (qualifier value)
Below reference range
active
true
activeDate
Jan 31, 2002
effectiveDate
Jan 31, 2002
moduleId
900000000000207008
definitionStatusId
900000000000074008
has interpretation
(1229882003) 11q22.2q22.3 microdeletion syndrome (1229883008) 19p13.3 microduplication syndrome (disorder) (1228844002) 1p35.2 microdeletion syndrome (167372005) 24 hour urine volume reduced (733637001) 3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) (1228886008) 9q33.3q34.11 microdeletion syndrome (5967006) A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis (89810003) A>gamma< delta beta^0^ Thalassemia (71988008) Aase syndrome (125127009) Abnormally decreased organ weight (241969009) Accidental hypothermia in elderly person (718573009) Achalasia microcephaly syndrome (disorder) (80875006) Achlorhydric anemia (789175008) Acidity of faeces abnormally low (721283000) Acidosis due to type 1 diabetes mellitus (disorder) (721284006) Acidosis due to type 2 diabetes mellitus (disorder) (55907008) Acquired aplastic anemia (735440005) Acquired eosinopenia (disorder) (307343001) Acquired hemoglobin H disease (4854004) Acquired hemolytic anemia (421851008) Acquired hemolytic anemia associated with AIDS (disorder) (713533000) Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder) (1148856007) Acquired iron deficiency anaemia due to increased requirement in infancy (724557008) Acquired iron deficiency anemia due to decreased absorption (disorder) (717948004) Acquired iron deficiency anemia due to increased iron requirement (disorder) (735443007) Acquired lymphocytopenia (disorder) (1156296001) Acquired neutropenia (191345000) Acquired neutropenia in newborn (5876000) Acquired pancytopenia (234376007) Acquired red cell aplasia (191228007) Acquired spherocytosis (721295000) Acquired thiamine deficiency anemia (disorder) (74576004) Acquired thrombocytopenia (439007008) Acquired thrombotic thrombocytopenic purpura (disorder) (26944003) Acute megaloblastic anemia due to dialysis (710134003) Acute muscle stiffness of neck (finding) (1081801000112104) Acute nephrotic syndrome (disorder) (57192008) Acute pure red cell aplasia (1153413001) Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) (444108000) Acute sickle cell splenic sequestration crisis (disorder) (1153415008) Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis (784392009) Adult chronic idiopathic neutropenia (disorder) (765748009) Adult pure red cell aplasia (disorder) (119249001) Agammaglobulinemia (722281001) Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) (237641009) Alcohol-induced hypoglycaemia (14333004) Alloimmune neonatal neutropenia (128094006) Alloimmune platelet transfusion refractoriness (128093000) Alloimmune thrombocytopenia (715342005) Alpha thalassemia X-linked intellectual disability syndrome (disorder) (234385007) Alpha thalassemia-2 trait (191187006) Alpha trait thalassemia (234389001) Alpha-beta thalassemia (166562001) Alpha-fetoprotein low (734349003) Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) (720982007) Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) (234482009) Amegakaryocytic thrombocytopenia (359531004) Amegakaryocytic thrombocytopenia with congenital malformation (702437000) Amish lethal microcephaly (disorder) (713496008) Anaemia caused by zidovudine (713349004) Anaemia co-occurrent with human immunodeficiency virus infection (129232009) Analbuminemia (136281000119109) Anemia caused by antineoplastic agent (691401000119104) Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder) (691411000119101) Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder) (44288006) Anemia due to abnormality extrinsic to the red cell (127319005) Anemia due to alloimmune destruction of transfused red cells (14514008) Anemia due to disturbance of hemoglobin synthesis (111577008) Anemia due to enzyme deficiency (43707008) Anemia due to heat (36919001) Anemia due to lead (34247008) Anemia due to mechanical damage (111575000) Anemia due to membrane defect (29177004) Anemia due to pentose phosphate pathway defect (53743006) Anemia following fetal blood loss (47100003) Anemia of prematurity (720986005) Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) (249912007) Ankle stiff (720494009) Anonychia with microcephaly syndrome (disorder) (713910008) Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder) (66309005) Antibody-mediated anemia (720498007) Aphalangy and syndactyly with microcephaly syndrome (disorder) (306058006) Aplastic anaemia (713508003) Aplastic anaemia co-occurrent with human immunodeficiency virus infection (191248000) Aplastic anaemia due to toxic cause (421102007) Aplastic anemia associated with AIDS (disorder) (413565006) Aplastic anemia associated with metabolic alteration (disorder) (413566007) Aplastic anemia associated with pancreatitis (disorder) (413567003) Aplastic anemia associated with pregnancy (disorder) (118791000119106) Aplastic anemia caused by antineoplastic agent (191244003) Aplastic anemia due to chronic disease (267527002) Aplastic anemia due to drugs (191246001) Aplastic anemia due to infection (191247005) Aplastic anemia due to radiation (768556005) Ataxia pancytopenia syndrome (789660001) Atypical haemolytic uraemic syndrome (276580005) Atypical isoimmunization of newborn (413603009) Autoimmune hemolytic anemia (disorder) (91411007) Autoimmune hemolytic anemia due to IgA (33491002) Autoimmune hemolytic anemia due to IgA plus complement (5603006) Autoimmune hemolytic anemia due to IgG (62609001) Autoimmune hemolytic anemia due to IgG plus complement (71832003) Autoimmune hemolytic anemia due to IgM (11781007) Autoimmune hemolytic anemia due to complement (718716008) Autoimmune hemolytic anemia mixed type (disorder) (127061005) Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement (71858003) Autoimmune hypoglycemia (123777002) Autoimmune leukopenia (276575001) Autoimmune neonatal thrombocytopenia (234425008) Autoimmune neutropenia (183005) Autoimmune pancytopenia (128091003) Autoimmune thrombocytopenia (438476003) Autoimmune thrombotic thrombocytopenic purpura (disorder) (720521008) Autosomal dominant macrothrombocytopenia (disorder) (725050005) Autosomal dominant osteopetrosis type 2 (disorder) (778070003) Autosomal dominant primary microcephaly (770947009) Autosomal dominant severe congenital neutropaenia (1187252002) Autosomal dominant thrombocytopenia with platelet secretion defect (770404004) Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) (784381008) Autosomal recessive cutis laxa type 2A (disorder) (778068007) Autosomal recessive cutis laxa type 2B (715981004) Autosomal recessive primary microcephaly (disorder) (783201001) Autosomal recessive severe congenital neutropenia due to CSF3R deficiency (783200000) Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency (783199003) Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency (783058007) Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency (disorder) (1003473002) B cell lymphocyte aplasia caused by drug (disorder) (102634007) Base deficit (1156292004) Basophil count below reference range (finding) (75654009) Benign autosomal dominant osteopetrosis (1156300000) Benign ethnic neutropenia (disorder) (128090002) Benign gestational thrombocytopenia (129640007) Benign granulocytopenia in childhood (54569005) Bernard Soulier syndrome (269175006) Beta thalassaemia trait (718196002) Beta thalassemia X-linked thrombocytopenia syndrome (disorder) (191189009) Beta thalassemia intermedia (1197589000) Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder) (15634931000119109) Bilateral stiffness of knee joints (disorder) (783194008) Bleeding diathesis due to thromboxane synthesis deficiency (1157018000) Blood oxygen concentration below reference range (860749004) Blood substance level low (finding) (846676008) Body temperature below reference range (449781000) Bone density below reference range (254113006) Bruck syndrome (167744001) CSF: chloride decreased (167751005) CSF: globulin decreased (167740005) CSF: glucose decreased (1220595008) Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) (50220002) Cellular immunologic aplastic anemia (726669007) Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder) (298234007) Cervical spine stiff (314645002) Child HC 0.5th - 1.9th centile (314643009) Child HC < 0.4th centile (314644003) Child HC = 0.4th centile (314646001) Child HC = 2nd centile (705065000) Childhood nephrotic syndrome (disorder) (276628009) Chloramphenicol-induced neutropenia (702354007) Christianson syndrome (90414007) Chronic acquired pure red cell aplasia (234418001) Chronic benign granulocytopenia (234423001) Chronic benign neutropenia (129641006) Chronic benign neutropenia of childhood (127055007) Chronic cold agglutinin disease (127056008) Chronic cold agglutinin disease associated with B-cell neoplasm (88854002) Chronic constitutional pure red cell aplasia (707480001) Chronic hemolytic anemia (disorder) (129643009) Chronic hypoplastic neutropenia (22098000) Chronic idiopathic autoimmune hemolytic anemia (129642004) Chronic idiopathic immunoneutropenia in adults (234576008) Chronic idiopathic neutropenia (248693006) Chronic idiopathic neutropenia (13172003) Chronic idiopathic thrombocytopenic purpura (763130006) Cleft palate, large ears, small head syndrome (127054006) Cold agglutinin disease due to Epstein-Barr virus infection (398937006) Cold autoimmune hemolytic anemia (disorder) (389199001) Cole-Carpenter dysplasia (disorder) (165433009) Color index low (1197428008) Combined immunodeficiency, enteropathy spectrum (80251000119104) Complement level below reference range (1228858000) Complex lethal osteochondrodysplasia (disorder) (716336002) Congenital amegakaryocytic thrombocytopenia (disorder) (63565007) Congenital anemia (111571009) Congenital atransferinemia (1208617001) Congenital autosomal recessive small-platelet thrombocytopenia (disorder) (71901000) Congenital contracted pelvis (716698007) Congenital deficiency of alpha-fetoprotein (disorder) (52951008) Congenital dyserythropoietic anemia (719453009) Congenital dyserythropoietic anemia type IV (disorder) (59548005) Congenital dyserythropoietic anemia, type I (68870007) Congenital dyserythropoietic anemia, type II (26409005) Congenital dyserythropoietic anemia, type III (441134009) Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder) (1174000008) Congenital generalized hypercontractile muscle stiffness syndrome (42601008) Congenital hemolytic anemia (444976001) Congenital hemolytic uremic syndrome (disorder) (267460002) Congenital hypogammaglobulinaemia (1197059004) Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) (722390006) Congenital intrauterine infection-like syndrome (disorder) (1142087002) Congenital megaloblastic anemia due to transcobalamin II deficiency (disorder) (1148758003) Congenital microcephaly (disorder) (782757004) Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (48796009) Congenital nephrotic syndrome (722118005) Congenital nephrotic syndrome due to congenital infection (disorder) (722369003) Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) (236384008) Congenital nephrotic syndrome with focal glomerulosclerosis (733453005) Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome (89655007) Congenital neutropenia (775909002) Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder) (363041004) Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (765327005) Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (737221003) Congenital thrombocytopenia (disorder) (267535004) Congenital thrombocytopenic purpura (234353009) Congenital transferrin deficiency (28975000) Constitutional aplastic anemia (267524009) Constitutional aplastic anemia with malformation (735439008) Constitutional eosinopenia (disorder) (871005) Contracted pelvis (12189000) Coombs negative hemolytic anemia (74789008) Coombs positive hemolytic anemia (1217229007) Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) (278833002) Craniometadiaphyseal dysplasia (725099009) Craniometadiaphyseal dysplasia wormian bone type (disorder) (1153488003) Creatine kinase below reference range (863930006) Creatinine clearance decreased (722453009) Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) (48788004) Cyclic thrombocytopenia (191347008) Cyclical neutropenia (50820005) Cytopenia (735457009) Cytopenia caused by drug (finding) (1172604004) DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome (719021005) DK phocomelia syndrome (disorder) (350353007) De Vaal's syndrome (131059003) Decreased 11-deoxy, 17-hydroxycorticosterone level (131056005) Decreased 11-deoxycorticosterone level (124803004) Decreased 17-ketogenic steroids level (131050004) Decreased 17-ketosteroids level (131099000) Decreased 3,3' diiothyronine level (124089001) Decreased adenylic acid (131044009) Decreased adrenal cortical hormone level (131012005) Decreased adrenocorticotropic hormone level (127355002) Decreased albumin (124023002) Decreased alpha-globulin (124026005) Decreased alpha1 globulin (124057005) Decreased amino acid (131075000) Decreased androgen level (124033005) Decreased angiotensin II level (131029008) Decreased anti-diuretic hormone level (55973006) Decreased arterial wedge pressure (131129005) Decreased ascorbic acid (124060003) Decreased beta amino isobutyric acid (124036002) Decreased beta globulin (124078008) Decreased bilirubin level (131131001) Decreased biotin (418928000) Decreased blood eosinophil number (finding) (419188005) Decreased blood leukocyte number (finding) (123823007) Decreased blood oxygen pressure (110373000) Decreased bone marrow iron (123996009) Decreased carbohydrate (131176001) Decreased carboxyhaemoglobin (131112007) Decreased carotene (124051006) Decreased cerebroside (124055002) Decreased cholesterol esters (127352004) Decreased choline (124074005) Decreased coproporphyrin (131087007) Decreased corticosterone level (131003008) Decreased corticotropin releasing factor level (131081008) Decreased cortisol level (131084000) Decreased cortisone level (124062006) Decreased cystine (131035008) Decreased epinephrine level (131066002) Decreased estradiol level (131069009) Decreased estriol level (131063005) Decreased estrone level (131177005) Decreased fibrinogen (87066005) Decreased fibrinolysis (131133003) Decreased folic acid (123998005) Decreased fructose (124004009) Decreased galactose (124053009) Decreased ganglioside (124020004) Decreased globulin (131107006) Decreased glucagon level (51798006) Decreased glucose level (124012001) Decreased glycogen (124064007) Decreased histidine (131101007) Decreased human chorionic gonadotropin level (131006000) Decreased human growth hormone level (131137002) Decreased immunoglobulin (131104004) Decreased insulin level (124001001) Decreased lactose (124043008) Decreased lipid (124041005) Decreased lipoprotein (124007002) Decreased mannoheptulose (131015007) Decreased melanocyte stimulating hormone level (131172004) Decreased methaemoglobin (124017007) Decreased methemalbumin (131038005) Decreased norepinephrine level (123987009) Decreased orotic acid (131032006) Decreased oxytocin level (131135005) Decreased pantothenic acid (7206008) Decreased peak expiratory flow rate (124009004) Decreased pentose (124046000) Decreased phospholipid (131020007) Decreased pituitary follicle stimulating hormone (131026001) Decreased pituitary gonadotropin level (131023009) Decreased pituitary luteinizing hormone level (84697003) Decreased plasma volume (124068005) Decreased porphyrin (131073007) Decreased pregnanediol level (131070005) Decreased pregnanetriol level (131053002) Decreased progesterone level (131009007) Decreased prolactin level (131000006) Decreased protein hormone level (124030008) Decreased protein-bound iodine (124077003) Decreased protoporphyrin (131108001) Decreased secretin level (131140002) Decreased serotonin level (60439007) Decreased serum protein level (124048004) Decreased sphingomyelin (131174003) Decreased sulfhemoglobin (131078003) Decreased testosterone level (131090001) Decreased thyroid hormone level (131017004) Decreased thyroid stimulating hormone level (131093004) Decreased thyroxine level (131096007) Decreased triiodothyronine level (124066009) Decreased tyrosine (63192007) Decreased uric acid level (718403007) Decreased urine output (finding) (124086008) Decreased urobilin (124082005) Decreased urobilinogen level (124071002) Decreased uroporphyrin (131041001) Decreased vanillylmandelic acid level (607007) Decreased vital capacity (131110004) Decreased vitamin A (131125004) Decreased vitamin B (131127007) Decreased vitamin B12 (131114008) Decreased vitamin D (127356001) Decreased vitamin E (131117001) Decreased vitamin K (131121008) Decreased vitamin K1 (131123006) Decreased vitamin K2 (123991004) Decreased xanthine (130197005) Deficiency of N-acetylgalactosamine-6-sulfatase (717185008) Deficiency of leukotriene C4 synthase (disorder) (234388009) Delta-beta-Lepore thalassaemia (26298008) Diabetic coma with ketoacidosis (111556005) Diabetic ketoacidosis without coma (389214003) Diaphyseal dysplasia with anemia (disorder) (373421000) Diarrhea-associated hemolytic uremic syndrome (disorder) (373422007) Diarrhea-negative hemolytic uremic syndrome (disorder) (782737003) Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (51624005) Dilutional thrombocytopenia (38970002) Doan-Wright syndrome (716682000) Dominant beta-thalassemia (disorder) (56918001) Dose-related drug-induced neutropenia (720598005) Doughnut lesion of calvaria and bone fragility syndrome (disorder) (236385009) Drash syndrome (441322009) Drug induced thrombotic thrombocytopenic purpura (disorder) (309742004) Drug-induced autoimmune hemolytic anemia (15276008) Drug-induced enzyme deficiency anemia (237640005) Drug-induced hypoglycemia (190448007) Drug-induced hypoglycemia without coma (127060006) Drug-induced immune hemolytic anemia, hapten type (18323000) Drug-induced immune hemolytic anemia, immune complex type (19307009) Drug-induced immune thrombocytopenia (47318007) Drug-induced neutropenia (1148880006) Drug-induced non autoimmune haemolytic anaemia (307337003) Duffy isoimmunisation of the newborn (111231000119109) Dyslipidemia with high density lipoprotein below reference range and triglyceride above reference range due to type 2 diabetes mellitus (254104009) Dysplasia with decreased bone density (165466008) ESR low (1169356004) Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) (237642002) Ectopic IGF hypoglycemia (237643007) Ectopic IGF-1 hypoglycaemia (237644001) Ectopic IGF-2 hypoglycemia (249917001) Elbow stiff (254130008) Endosteal hyperostoses (254132000) Endosteal hyperostoses with cerebellar hypoplasia (43355006) Eosinopenia (860827002) Eosinopenia due to infectious disease (disorder) (733031004) Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) (721975004) Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) (25502009) Episodic lymphocytopenia (46760003) Estren-Dameshek anemia (1172725005) Euglobulin clot lysis time below reference range (finding) (75331009) Evans syndrome (771179007) Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder) (167653002) Faecal lipase reduced (167655009) Faecal tryptic activity low (722721004) Familial haemolytic uraemic syndrome (718141008) Familial idiopathic steroid-resistant nephrotic syndrome (disorder) (360495000) Familial megaloblastic anemia (236383002) Familial mesangial sclerosis (247860002) Familial neutropenia (1187040004) Familial steroid-resistant nephrotic syndrome with adrenal insufficiency (783614008) Familial steroid-resistant nephrotic syndrome with sensorineural deafness (disorder) (30575002) Fanconi's anemia (6974005) Fasting hypoglycemia (426800001) Febrile granulocytopenia (disorder) (427245000) Febrile leukopenia (disorder) (409089005) Febrile neutropenia (disorder) (1162362005) Felty syndrome with seronegative erosive rheumatoid arthritis (disorder) (1162364006) Felty syndrome with seronegative rheumatoid arthritis (disorder) (57160007) Felty's syndrome (165626000) Ferritin level low (431265009) Fetal microcephaly (disorder) (10752381000119101) Fetal thrombocytopenia (720954000) Filippi syndrome (disorder) (298238005) Finger joint stiff (197601003) Finnish congenital nephrotic syndrome (298241001) Foot joint stiff (22933009) G-6-PD class I variant anemia (34852006) G-6-PD class II variant anemia (24661004) G-6-PD class III variant anemia (82003006) G-6-PD class IV variant anemia (80963002) G-6-PD class V variant anemia (86859003) G-6-PD variant enzyme deficiency anemia (713388002) GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) (721297008) Galloway Mowat syndrome (disorder) (788944005) Gamma delta beta thalassemia (234390005) Gamma thalassaemia (199405005) Generally contracted pelvis - delivered (199406006) Generally contracted pelvis with antenatal problem (254116003) Geroderma osteodysplastica (863929001) Glomerular filtration rate decreased (62403005) Glucose-6-phosphate dehydrogenase deficiency anemia (717822006) Goldberg Shprintzen megacolon syndrome (disorder) (166382003) Gonadotrophin levels low (416955003) Granulocyte count below reference range (finding) (417672002) Granulocytopenic disorder (disorder) (95605009) HELLP syndrome (47526003) HNSHA due to NADH diaphorase deficiency (78908001) HNSHA due to decreased adenosine deaminase activity (62268000) HNSHA due to diphosphoglycerate mutase deficiency (25251008) HNSHA due to gamma glutamyl cysteine synthetase deficiency (52413004) HNSHA due to glucose phosphate isomerase deficiency (52212006) HNSHA due to glutathione reductase deficiency (111579006) HNSHA due to glutathione synthetase deficiency (42484009) HNSHA due to hexokinase deficiency (5315003) HNSHA due to increased adenosine deaminase activity (41387000) HNSHA due to phosphofructokinase deficiency (59644002) HNSHA due to phosphoglycerate kinase deficiency (34194007) HNSHA due to pyrimidine-5'-nucleotidase deficiency (74703006) HNSHA due to pyruvate kinase deficiency (44641000) HNSHA due to triosephosphate isomerase deficiency (39586009) HPFH A gamma beta^+^ thalassemia (61395005) HPFH G gamma beta^+^ thalassemia (85557000) HPFH deletion type (54006005) HPFH delta beta^0^ thalassemia (89459006) HPFH linked to beta-globulin gene cluster (56205004) HPFH nondeletion type (32855007) HPFH unlinked to beta-globulin gene cluster (719395001) Hadziselimovic syndrome (234386008) Haemoglobin Constant Spring trait (1148897000) Haemoglobin Paksé disease (191222008) Haemoglobinuria due to haemolysis from external causes (1142083003) Haemolytic anaemia of pregnancy (721008000) Hall Riggs syndrome (disorder) (249915009) Hand joint stiff (86225009) Hapten type high affinity hemolytic anemia (44206008) Hapten type low affinity hemolytic anemia (69216008) Hb Lepore thalassemia (127040003) Hb S disease (165414004) Hematocrit - PCV - low (5300004) Hemoglobin Bart's hydrops syndrome (119691000119106) Hemoglobin C/beta thalassemia disease (disorder) (119701000119106) Hemoglobin D/beta thalassemia disease (disorder) (234392002) Hemoglobin E/beta thalassemia disease (447117006) Hemoglobin H constant spring thalassemia (disorder) (48553001) Hemoglobin H disease (234387004) Hemoglobin Lepore trait (417425009) Hemoglobin SS disease with crisis (disorder) (440206000) Hemoglobin SS disease with vasoocclusive crisis (disorder) (416180004) Hemoglobin SS disease without crisis (disorder) (1148899002) Hemoglobin Seal Rock disease (disorder) (165397008) Hemoglobin low (61261009) Hemolytic anemia (76366001) Hemolytic anemia due to Bartonella (28147001) Hemolytic anemia due to Clostridium welchii (766982000) Hemolytic anemia due to adenylate kinase deficiency (disorder) (24620004) Hemolytic anemia due to babesiosis (81711008) Hemolytic anemia due to drugs (191170009) Hemolytic anemia due to glutathione metabolism disorder (1148893001) Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency (191177007) Hemolytic anemia due to hexokinase deficiency (129638002) Hemolytic anemia due to hyperbaric oxygen (38689004) Hemolytic anemia due to infection (77663007) Hemolytic anemia due to malaria (4939006) Hemolytic anemia due to nonlymphoid neoplasm (1148895008) Hemolytic anemia due to red cell enolase deficiency (disorder) (191179005) Hemolytic anemia due to triose phosphate isomerase deficiency (60805002) Hemolytic anemia with emphysema AND cutis laxa (32858009) Hemolytic disease of fetus OR newborn due to ABO immunization (86986002) Hemolytic disease of fetus OR newborn due to Rh isoimmunization (387705004) Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) (350611000119107) Hemolytic disease of fetus due to ABO immunization (350601000119109) Hemolytic disease of newborn due to ABO immunization (disorder) (111469006) Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization (111407006) Hemolytic uremic syndrome (36568005) Hemolytic uremic syndrome of childhood (78209002) Hemolytic uremic syndrome, adult type (73397007) Heparin-induced thrombocytopenia (111588002) Heparin-induced thrombocytopenia with thrombosis (773489008) Hereditary cryohydrocytosis with normal stomatin (disorder) (782911008) Hereditary cryohydrocytosis with reduced stomatin (191169008) Hereditary elliptocytosis (75443009) Hereditary elliptocytosis due to abnormal protein 4.1 (8857001) Hereditary elliptocytosis due to alpha spectrin defect (73073009) Hereditary elliptocytosis due to beta spectrin defect in self-association (66262001) Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (5994005) Hereditary elliptocytosis due to deficiency of protein 4.1 (15121005) Hereditary elliptocytosis due to glycophorin C deficiency (234410008) Hereditary elliptocytosis with transient poikilocytosis (735453008) Hereditary folate deficiency anemia (disorder) (38911009) Hereditary hemolytic anemia (1153403009) Hereditary iron deficiency anemia (783255002) Hereditary isolated aplastic anemia (301317008) Hereditary nonspherocytic haemolytic anaemia (16964007) Hereditary persistence of fetal hemoglobin thalassemia (55995005) Hereditary spherocytosis (69981004) Hereditary spherocytosis due to beta spectrin defect (47516005) Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (33905008) Hereditary spherocytosis due to deficiency of protein 4.2 (25266006) Hereditary spherocytosis due to spectrin deficiency (14087004) Hereditary stomatocytosis (1172699002) Hereditary thrombocytopenia with early-onset myelofibrosis (783251006) Hereditary thrombocytopenia with normal platelets (438492008) Hereditary thrombocytopenic disorder (disorder) (735452003) Hereditary vitamin B12 deficiency anemia (disorder) (19442009) Heterozygous thalassemia (249914008) Hip stiff (234383000) Homozygous alpha thalassemia (26682008) Homozygous beta thalassemia (119641000119103) Homozygous hemoglobin H constant spring thalassemia (disorder) (1153399000) Homozygous hereditary elliptocytosis (disorder) (14024008) Humoral immunologic aplastic anemia (78071008) Hydromicrocephaly (1217210001) Hyperostosis cranialis interna (disorder) (59763006) Hyperphosphatasemia tarda (1148928001) Hypocalcemia due to chronic kidney disease (disorder) (711161006) Hypochromic microcytic anemia with iron overload (disorder) (16318061000119108) Hypogammaglobulinaemia due to monoclonal gammopathy of undetermined significance (16318001000119107) Hypogammaglobulinaemia due to multiple myeloma (119250001) Hypogammaglobulinemia (302866003) Hypoglycaemia (237632004) Hypoglycaemic event in diabetes (120711000119108) Hypoglycaemic unawareness in type 1 diabetes mellitus (84371000119108) Hypoglycemia due to type 1 diabetes mellitus (120731000119103) Hypoglycemia due to type 2 diabetes mellitus (disorder) (68581004) Hypoglycemia of childhood (119831000119106) Hypoglycemia unawareness in type 2 diabetes mellitus (disorder) (719216001) Hypoglycemic coma co-occurrent and due to diabetes mellitus type II (disorder) (421725003) Hypoglycemic coma in diabetes mellitus (disorder) (421437000) Hypoglycemic coma in type I diabetes mellitus (disorder) (237630007) Hypoglycemic disorder (360546002) Hypoglycemic shock (237633009) Hypoglycemic state in diabetes (773665006) Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (disorder) (773666007) Hypoinsulinemic hypoglycemia and body hemihypertrophy (762434003) Hypomagnesuria (1148926002) Hypophosphatemia due to chronic kidney disease (disorder) (41614006) Hypoplastic anemia (386689009) Hypothermia (finding) (212916004) Hypothermia - accidental (269287005) Hypothermia due to anaesthetic (83966006) Hypothermia due to cold environment (123461000119109) Hypothermia not associated with low environmental temperature (13629008) Hypothermia of newborn (47872005) Hypoviscosity (1208747005) ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement (1137328006) Iatrogenic hypoglycaemia (276562001) Iatrogenic neonatal hypoglycemia (191256002) Idiopathic aplastic anaemia (6398009) Idiopathic chronic cold agglutinin disease (371106008) Idiopathic maternal thrombocytopenia (disorder) (62871001) Idiopathic paroxysmal cold hemoglobinuria (276448005) Idiopathic sideroblastic anemia (241968001) Immersion hypothermia (277892007) Immobility stiffness (1186654001) Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder) (65623009) Immune neutropenia (2897005) Immune thrombocytopenia (77084001) Immunologic aplastic anemia (398052002) Induced hypothermia (finding) (770725000) Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (367489004) Infantile malignant osteopetrosis (724226009) Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) (1197476009) Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia (disorder) (36854009) Inlet contraction of pelvis (199409004) Inlet pelvic contraction - delivered (199410009) Inlet pelvic contraction with antenatal problem (84361000119102) Insulin reactive hypoglycemia in type 2 diabetes mellitus (773552008) Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (722455002) Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder) (1208746001) Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (298244009) Interphalangeal joint of toe stiff (322699009) Intracorpuscular haemolytic anaemia (1177178005) Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) (1197592001) Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome (1148861009) Iron deficiency anaemia due to coeliac disease (191128004) Iron deficiency anaemia due to dietary causes (87522002) Iron deficiency anemia (724556004) Iron deficiency anemia due to blood loss (disorder) (1148855006) Iron deficiency anemia due to increased requirement in adolescence (disorder) (1148853004) Iron deficiency anemia following gastrectomy (disorder) (10812081000119108) Iron deficiency anemia in mother complicating childbirth (199248002) Iron deficiency anemia of pregnancy (371315009) Iron deficiency anemia secondary to inadequate dietary iron intake (disorder) (722005000) Iron-refractory iron deficiency anemia (disorder) (78378009) Isoimmune neutropenia (724637001) Isolated thrombocytopenia (disorder) (771470001) Jawad syndrome (84445001) Joint stiffness (298232006) Joint stiffness of spine (240156000) Juvenile idiopathic generalized osteoporosis (49284006) Juvenile type megaloblastic anemia (86635005) Kasabach-Merritt syndrome (234380002) Kell isoimmunization of the newborn (420422005) Ketoacidosis in diabetes mellitus (disorder) (420270002) Ketoacidosis in type I diabetes mellitus (disorder) (421750000) Ketoacidosis in type II diabetes mellitus (disorder) (421075007) Ketoacidotic coma in type I diabetes mellitus (disorder) (421847006) Ketoacidotic coma in type II diabetes mellitus (disorder) (20825002) Ketotic hypoglycemia (307338008) Kidd isoimmunization of the newborn (249913002) Knee stiff (770942003) Kostmann syndrome (disorder) (1217208003) L-ferritin deficiency (disorder) (771447009) LAMB2-related infantile-onset nephrotic syndrome (735538002) Lactic acidosis co-occurrent and due to diabetes mellitus (disorder) (276579007) Late anaemia of newborn (206434001) Late anaemia of newborn due to isoimmunisation (68361004) Late anemia due to isoimmunization (863932003) Left ventricular ejection fraction decreased (783157004) Leigh syndrome with nephrotic syndrome (disorder) (1393001) Lenz-Majewski hyperostosis syndrome (719402008) Lethal hemolytic anemia and genital anomaly syndrome (disorder) (62151007) Leucine-induced hypoglycemia (84828003) Leukopenia (1148696006) Leukopenia caused by drug (170766006) Loss of hypoglycemic warning (441956008) Low cobalt level in blood (1169364005) Low density lipoprotein receptor-related protein 5 related primary osteoporosis (disorder) (126121000119104) Low serum ferritin (166449002) Low serum oestradiol levels (166690008) Low serum potassium level - finding (735930004) Low-level literacy (finding) (721974000) Lowry MacLean syndrome (disorder) (298236009) Lumbar spine stiff (1156294003) Lymphocyte count below reference range (1153358006) Lymphocyte passenger syndrome following organ transplantation (48813009) Lymphocytopenia (866151004) Lymphocytopenia due to COVID-19 (866084002) Lymphopenia due to infection (165439008) MCH - low (165447008) MCHC - low (165455001) MCV - low (712922002) MYH9 related disease (1142062009) Macrocytic anaemia of pregnancy (771075004) Macrothrombocytopenia with mitral valve insufficiency (1172685001) Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (703540008) Majeed syndrome (166455007) Male sex hormones low (190406000) Malnutrition-related diabetes mellitus with ketoacidosis (167941003) Marrow megakaryocyte decrease (234381003) Maternal autoimmune hemolytic anemia (80255009) Maternal transfer neutropenia (441918007) Maximal voluntary ventilation capacity below reference range (finding) (442686002) Measurement finding below reference range (finding) (1153380009) Mechanical haemolysis due to prosthetic valve (191217008) Mechanical haemolytic anaemia (60628003) Mediterranean macrothrombocytopenia (234487003) Mediterranean thrombocytopenia (359536009) Megakaryocytic aplasia (234483004) Megakaryocytic thrombocytopenia (87810006) Megaloblastic anemia due to alcoholism (60164003) Megaloblastic anemia due to blind loop syndrome (60504009) Megaloblastic anemia due to congenital deficiency of intrinsic factor (82895008) Megaloblastic anemia due to disease of small intestine (68700003) Megaloblastic anemia due to error of cobalamin metabolism (35778001) Megaloblastic anemia due to error of folate metabolism (721184003) Megaloblastic anemia due to folate deficiency due to increased requirement (disorder) (721185002) Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder) (721186001) Megaloblastic anemia due to folate deficiency in prematurity (disorder) (27798002) Megaloblastic anemia due to impaired absorption of folate (34925000) Megaloblastic anemia due to inborn errors of metabolism (6659005) Megaloblastic anemia due to nontropical sprue (91217009) Megaloblastic anemia due to pregnancy (87806008) Megaloblastic anemia due to tropical sprue (237617006) Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (59178007) Menkes kinky-hair syndrome (735539005) Metabolic acidosis co-occurrent and due to diabetes mellitus (disorder) (234424007) Metabolic neutropenia (298237000) Metacarpophalangeal joint stiff (298243003) Metatarsophalangeal joint stiff (51071000) Microangiopathic hemolytic anemia (1187195007) Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) (723404002) Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) (1208348002) Microcephalic osteodysplastic primordial dwarfism type II (725461009) Microcephalic osteodysplastic primordial dwarfism types I and III (disorder) (770564004) Microcephalic primordial dwarfism Alazami type (disorder) (770565003) Microcephalic primordial dwarfism Dauber type (765758008) Microcephalic primordial dwarfism Montreal type (715482004) Microcephalic primordial dwarfism of Toriello type (disorder) (1220596009) Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) (719380003) Microcephalus cardiomyopathy syndrome (disorder) (719394002) Microcephalus cleft palate syndrome (disorder) (715462003) Microcephalus co-occurrent with cervical spine fusion anomaly (disorder) (715464002) Microcephalus microcornea syndrome of Seemanova type (disorder) (719377004) Microcephalus with albinism and digital anomaly syndrome (disorder) (719378009) Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) (719379001) Microcephalus with cardiac defect and lung malsegmentation syndrome (disorder) (770655004) Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) (764732004) Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (763798008) Microcephalus, complex motor and sensory axonal neuropathy syndrome (733472005) Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) (733092009) Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) (733604003) Microcephalus, lymphedema, chorioretinopathy syndrome (1148757008) Microcephaly (finding) (716112005) Microcephaly with deafness and intellectual disability syndrome (disorder) (1003373003) Microcephaly with simplified gyral pattern (1172683008) Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (721903007) Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder) (715533002) Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder) (773305003) Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) (723304001) Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) (771074000) Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder) (770721009) Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder) (703369003) Microcephaly-capillary malformation syndrome (234349007) Microcytic anemia (44666001) Microcytic hypochromic anemia (4984008) Microcytic normochromic anemia (237257002) Midpelvic contraction (123720003) Mild cytopenia (24975009) Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (32648007) Mild hereditary spherocytosis due to spectrin deficiency (724138007) Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) (66095000) Mixed hypoglycemia (123721004) Moderate cytopenia (165539005) Monocytopenia (234486007) Montreal syndrome (40144003) Morning stiffness - joint (717760006) Multi-drug resistant nephrotic syndrome (disorder) (1208725005) Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome (202510005) Multiple stiff joints (24974008) Myelokathexis (725009002) Neck pain co-occurrent with neck stiffness following whiplash injury to neck (disorder) (234350007) Neonatal anemia (774083009) Neonatal autoimmune haemolytic anaemia (52767006) Neonatal hypoglycemia (95624007) Neonatal lymphocytopenia (82835005) Neonatal thrombocytopenia (89962000) Neonatal thrombocytopenia due to exchange transfusion (61744005) Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (240305000) Neonatal thrombocytopenia due to platelet alloimmunisation (1010297003) Neonatal vitamin B12 deficiency due to maternal vitamin B12 deficiency (52254009) Nephrotic syndrome (368911000119109) Nephrotic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III (disorder) (713695001) Nephrotic syndrome co-occurrent with human immunodeficiency virus infection (disorder) (71721000119101) Nephrotic syndrome due to type 1 diabetes mellitus (71441000119104) Nephrotic syndrome due to type 2 diabetes mellitus (197604006) Nephrotic syndrome in amyloidosis (197605007) Nephrotic syndrome in diabetes mellitus (197603000) Nephrotic syndrome in diseases EC (197606008) Nephrotic syndrome in malaria (197607004) Nephrotic syndrome in polyarteritis nodosa (363233007) Nephrotic syndrome secondary to glomerulonephritis (363234001) Nephrotic syndrome secondary to systemic disease (197591002) Nephrotic syndrome with membranoproliferative glomerulonephritis (197590001) Nephrotic syndrome with membranous glomerulonephritis (266549004) Nephrotic syndrome with minimal change glomerulonephritis (197589005) Nephrotic syndrome with proliferative glomerulonephritis (773647007) Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (197599000) Nephrotic syndrome, dense deposit disease (197600002) Nephrotic syndrome, diffuse crescentic glomerulonephritis (197597003) Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis (197595006) Nephrotic syndrome, diffuse membranous glomerulonephritis (197596007) Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis (197598008) Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis (197594005) Nephrotic syndrome, focal and segmental glomerular lesions (197593004) Nephrotic syndrome, minor glomerular abnormality (40233000) Nephrotic-nephritic syndrome (77817004) Neu-Laxova syndrome (237631006) Neuroglycopenia (767658000) Neutropaenia due to and following chemotherapy (165517008) Neutropenia (416729007) Neutropenia associated with AIDS (disorder) (111585004) Neutropenia associated with autoimmune disease (46359005) Neutropenia associated with infectious disease (267540007) Neutropenia due to irradiation (276576000) Neutropenia of the small for gestational age baby (41814009) Neutropenia with dysgranulopoiesis (725137007) Neutropenia, monocytopenia, deafness syndrome (disorder) (303011007) Neutropenic disorder (443980004) Neutropenic sepsis (disorder) (276529009) Newborn environmental hypothermia (766753005) Nijmegen breakage syndrome-like disorder (disorder) (237635002) Nocturnal hypoglycemia (3902000) Non dose-related drug-induced neutropenia (191216004) Non-autoimmune hemolytic anemia (237637005) Non-diabetic hypoglycemia (725057008) Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder) (1142030006) Nutritional anaemia of pregnancy (722056009) Oculocerebrofacial syndrome Kaufman type (disorder) (722055008) Oculopalatocerebral syndrome (disorder) (1003381002) Onycho-tricho-dysplasia neutropenia syndrome (1177179002) Oral-facial-digital syndrome with short stature and brachymesophalangia (763837007) Oro-facial digital syndrome type 14 (240453002) Oroya fever (50108000) Osteochondrodysplasia with osteopetrosis (15552004) Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (732954002) Osteopenia, intellectual disability, sparse hair syndrome (disorder) (1926006) Osteopetrosis (205503007) Osteopetrosis - delayed type (254121000) Osteopetrosis - intermediate type (773730002) Osteopetrosis hypogammaglobulinemia syndrome (disorder) (254122007) Osteopetrosis with renal tubular acidosis (722113001) Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) (69217004) Outlet contraction of pelvis (199413006) Outlet pelvic contraction - delivered (199414000) Outlet pelvic contraction with antenatal problem (449171008) Oxygen saturation below reference range (finding) (722207000) Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) (127034005) Pancytopenia (328381000119105) Pancytopenia caused by anticonvulsant (328371000119107) Pancytopenia caused by antithyroid drug (disorder) (16623961000119100) Pancytopenia caused by immunosuppressant (736024007) Pancytopenia caused by medication (disorder) (783142006) Pancytopenia due to IKZF1 mutations (328301000119102) Pancytopenia due to antineoplastic chemotherapy (disorder) (774071007) Pancytopenia with developmental delay syndrome (234367000) Pancytopenia with pancreatitis (415005004) Panleukopenia (disorder) (127057004) Paroxysmal cold hemoglobinuria (127058009) Paroxysmal cold hemoglobinuria associated with tertiary syphilis (1155726000) Partial thromboplastin time below reference range (finding) (240486003) Parvoviral aplastic crisis (387702001) Perinatal anemia (disorder) (273986001) Perinatal thrombocytopenia (1153333001) Pernicious anaemia due to autoimmune disorder (1217367007) Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder) (276578004) Physiological anemia of infancy (723449004) Pierson syndrome (disorder) (1153494006) Plasma creatine kinase below reference range (166791001) Plasma proteins low (165462005) Plasma viscosity low (415116008) Platelet count below reference range (finding) (441458001) Platelet count below reference range at birth (finding) (167959000) Pleural fluid SG low (80126007) Plummer-Vinson syndrome (772126000) Poikiloderma with neutropenia (40387008) Polyagglutinable erythrocyte syndrome (33183004) Post infectious thrombocytopenic purpura (127053000) Post-infectious cold agglutinin disease (35703006) Post-viral paroxysmal cold hemoglobinuria (1173998003) Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (73162004) Posttransfusion purpura (863953007) Primaquine sensitivity anaemia (127049002) Primary (idiopathic) autoimmune hemolytic anemia (778027003) Primary CD59 deficiency (191210005) Primary cold-type hemolytic anemia (123718001) Primary cytopenia (782825008) Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (782755007) Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) (191338000) Primary splenic neutropenia (267534000) Primary thrombocytopenia (191211009) Primary warm-type haemolytic anaemia (1208481000) Progressive cerebello-cerebral atrophy (disorder) (1172900005) Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome (1187303004) Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (716023007) Prominent glabella with microcephaly and hypogenitalism syndrome (disorder) (249789000) Proportionate short legs (165569003) Prothrombin time low (733086003) Pseudoprogeria syndrome (disorder) (721119004) Pseudothrombocytopenia (finding) (236530006) Pulmonic stenosis and congenital nephrosis (50715003) Pure red cell aplasia (191229004) Pyknocytosis, infantile (89647000) Pyknodysostosis (1220568003) QRICH1-related intellectual disability, chondrodysplasia syndrome (165423001) RBC count low (165656009) RBC folate low (85589009) Radial aplasia-thrombocytopenia syndrome (371074009) Radiation thrombocytopenia (disorder) (721882001) Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) (719162001) Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) (166891009) Random blood sugar low (721304007) Refractory thrombocytopenia (disorder) (111584000) Reticular dysgenesis (351287008) Reticular dysgenesis with congenital aleucocytosis (124961001) Reticulocytopenia (1172605003) Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (1220597000) Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (723512008) Revesz syndrome (disorder) (307333004) Rhesus isoimmunisation due to anti-D (307335006) Rhesus isoimmunisation due to anti-E (307336007) Rhesus isoimmunization due to anti-Cw (307334005) Rhesus isoimmunization due to anti-c (1222659003) Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) (165794004) Rubella antibody low - not immune (298240000) Sacroiliac joint stiff (1197148005) Sanjad Sakati syndrome (disorder) (17568006) Sclerosteosis (57917004) Seckel syndrome (43858000) Secondary aplastic anemia (732960002) Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus (127050002) Secondary autoimmune hemolytic anemia (732962005) Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) (732963000) Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder (732965007) Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) (732966008) Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) (128092005) Secondary autoimmune thrombocytopenia (191212002) Secondary cold-type hemolytic anemia (123719009) Secondary cytopenia (253130001) Secondary microcephaly (50253007) Secondary paroxysmal cold hemoglobinuria (154826009) Secondary thrombocytopenia (127052005) Secondary warm autoimmune hemolytic anemia (191213007) Secondary warm-type haemolytic anaemia (234363001) Selective malabsorption of cyanocobalamin (167773003) Semen volume low: 0.5-1 ml. (166652002) Serum 5-nucleotidase level low (166327007) Serum T3 level low (1153475001) Serum acid phosphatase below reference range (1153477009) Serum albumin below reference range (finding) (1153478004) Serum alkaline phosphatase below reference range (1153479007) Serum amino acid below reference range (finding) (1153483007) Serum androstenedione below reference range (finding) (1153486004) Serum bicarbonate below reference range (1153489006) Serum creatine kinase below reference range (166715006) Serum creatinine low (165650003) Serum folate low (1153531003) Serum inorganic phosphate below reference range (165623008) Serum iron low (1153564003) Serum progesterone below reference range (166778002) Serum proteins low (1153567005) Serum sodium below reference range (finding) (1153574000) Serum testosterone below reference range (1153577007) Serum thyroid stimulating hormone below reference range (finding) (165645009) Serum vitamin B12 low (166742007) Serum zinc level low (722213009) Severe X-linked intellectual disability Gustavson type (disorder) (1187614006) Severe autosomal recessive macrothrombocytopenia (disorder) (190996002) Severe combined immunodefiency with reticular dysgenesis (725463007) Severe congenital hypochromic anemia with ringed sideroblasts (disorder) (123722006) Severe cytopenia (722401001) Severe fever with thrombocytopenia syndrome virus (disorder) (1172629005) Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (10564005) Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (77413008) Severe hereditary spherocytosis due to spectrin deficiency (1208727002) Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) (774149004) Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (disorder) (1217372003) Severe myopia, generalized joint laxity, short stature syndrome (771303004) Severe neonatal onset encephalopathy with microcephaly (disorder) (1179282009) Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (37492005) Sex-linked thrombocytopenia (1197586007) Short stature, advanced bone age, early-onset osteoarthritis syndrome (1187277001) Short stature, brachydactyly, obesity, global developmental delay syndrome (249918006) Shoulder stiff (89454001) Shwachman syndrome (10759351000119103) Sickle cell anaemia in mother complicating childbirth (127045008) Sickle cell anemia with coexistent alpha-thalassemia (234391009) Sickle cell anemia with high hemoglobin F (127046009) Sickle cell trait with coexistent alpha-thalassemia (127041004) Sickle cell-beta-thalassemia (127042006) Sickle cell-beta^+^-thalassemia (127043001) Sickle cell-beta^0^-thalassemia (127044007) Sickle cell-delta beta^0^-thalassemia (36472007) Sickle cell-thalassemia disease (416826005) Sickle cell-thalassemia disease with crisis (disorder) (417048006) Sickle cell-thalassemia disease without crisis (disorder) (290246007) Sideropenic anemia with reticuloendothelial siderosis (254114000) Singleton-Merten syndrome (733468006) Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome (167787003) Sperm motility 6-8 hours low - 10-30% (167779004) Sperm number/cc low: 10-30 million (167780001) Sperm number/cc very low: 0-10 million (715653007) Spondyloocular syndrome (disorder) (111559003) Spontaneous hypoglycemia (763717004) Sporadic fetal brain disruption sequence (717191005) Sporadic idiopathic steroid-resistant nephrotic syndrome (disorder) (449820008) Steroid resistant nephrotic syndrome of childhood (445119005) Steroid sensitive nephrotic syndrome of childhood (disorder) (236382007) Steroid-dependent nephrotic syndrome (236381000) Steroid-resistant nephrotic syndrome (236380004) Steroid-sensitive nephrotic syndrome (249921008) Stiff back (225609009) Stiff legs (225610004) Stiff limbs (161882006) Stiff neck (161880003) Stiff neck symptom (271587009) Stiffness (15745001000119105) Stiffness of bilateral ankle joints (finding) (15636851000119100) Stiffness of bilateral hand joints (finding) (15744041000119106) Stiffness of bilateral hip joints (finding) (15636811000119101) Stiffness of bilateral shoulder joints (finding) (450351000124108) Stiffness of bilateral wrist joints (finding) (15744881000119108) Stiffness of joint of bilateral foot regions (finding) (321891000119105) Stiffness of joint of left elbow (321901000119109) Stiffness of joint of left foot (321911000119107) Stiffness of joint of left hand (finding) (321921000119100) Stiffness of joint of left hip (finding) (321811000119101) Stiffness of joint of right elbow (finding) (321821000119108) Stiffness of joint of right foot (finding) (321831000119106) Stiffness of joint of right hand (321841000119102) Stiffness of joint of right hip (finding) (15745841000119104) Stiffness of joints of bilateral elbows (finding) (321881000119107) Stiffness of left ankle (finding) (321931000119102) Stiffness of left knee (finding) (321941000119106) Stiffness of left shoulder (finding) (321951000119108) Stiffness of left wrist (finding) (321801000119104) Stiffness of right ankle (finding) (321851000119100) Stiffness of right knee (finding) (321861000119103) Stiffness of right shoulder (finding) (321871000119109) Stiffness of right wrist (finding) (733072002) Stimmler syndrome (298242008) Subtalar joint stiff (167889008) Synovial fluid viscosity low (295111000119108) Systemic lupus erythematosus co-occurrent and due to nephrotic syndrome (disorder) (773554009) THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome (165630002) TIBC - Total iron binding capacity low (1172626003) Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) (298231004) Temporomandibular joint stiff (40108008) Thalassemia (10806241000119108) Thalassemia in mother complicating childbirth (72331000119105) Thalassemia in mother complicating pregnancy (934007) Thalassemia intermedia (75451007) Thalassemia major (84188003) Thalassemia syndrome (47047009) Thalassemia with other hemoglobinopathy (61777009) Thalassemia-hemoglobin C disease (12907000) Thiamine-responsive megaloblastic anemia (298235008) Thoracic spine stiff (1155725001) Thrombin time below reference range (finding) (97571000119109) Thrombocytopaenia co-occurrent and due to alcoholism (711407000) Thrombocytopathy, asplenia and miosis (disorder) (421766003) Thrombocytopenia associated with AIDS (disorder) (866152006) Thrombocytopenia due to COVID-19 (699208000) Thrombocytopenia due to alcohol (49886003) Thrombocytopenia due to blood loss (82190001) Thrombocytopenia due to defective platelet production (78345002) Thrombocytopenia due to diminished platelet production (191322006) Thrombocytopenia due to drugs (30182008) Thrombocytopenia due to extracorporal circulation (191323001) Thrombocytopenia due to extracorporeal circulation of blood (63444004) Thrombocytopenia due to hypersplenism (34395002) Thrombocytopenia due to hypothermia (307342006) Thrombocytopenia due to massive blood transfusion (87902006) Thrombocytopenia due to non-immune destruction (323079008) Thrombocytopenia due to sequestration (1187615007) Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) (302215000) Thrombocytopenic disorder (302873008) Thrombocytopenic purpura (417626001) Thrombocytopenic purpura associated with metabolic disorder (disorder) (402653004) Thrombocytopenic purpura due to defective platelet production (disorder) (402654005) Thrombocytopenic purpura due to platelet consumption (disorder) (78129009) Thrombotic thrombocytopenic purpura (298239002) Thumb joint stiff (733096007) Thyrocerebrorenal syndrome (123723001) Toxic cytopenia (191218003) Toxic hemolytic anemia (32092008) Toxic neutropenia (191255003) Transient acquired pure red cell aplasia (234375006) Transient erythroblastopenia of childhood (191251007) Transient hypoplastic anemia (449777000) Transient infantile osteopetrosis (735496003) Transient neonatal hypoglycemia due to hyperinsulinemia (disorder) (55444004) Transient neonatal neutropenia (722926003) Transient neonatal neutropenia co-occurrent and due to neonatal bacterial sepsis (finding) (722925004) Transient neonatal neutropenia due to congenital viral infection (finding) (23205009) Transient neonatal thrombocytopenia (206510008) Transient neonatal thrombocytopenia due to exchange transfusion (206511007) Transient neonatal thrombocytopenia due to idopathic maternal thrombocytopenia (206512000) Transient neonatal thrombocytopenia due to isoimmunisation (123724007) Transitory cytopenia (735497007) Transitory iatrogenic neonatal hypoglycemia (disorder) (276561008) Transitory neonatal hypoglycaemia (248996001) Transversely contracted pelvis (2835000) Traumatic cardiac hemolytic anemia (371046004) Traumatic hemolytic anemia (disorder) (237645000) Tumour-induced hypoglycaemia (762680008) Unplanned perioperative hypothermia (18273004) Unstable hemoglobin disease (373420004) Upshaw-Schulman syndrome (disorder) (416902009) Uremic thrombocytopenia (disorder) (167243006) Urine specific gravity low (1156746003) Vaccine-induced prothrombotic immune thrombocytopenia (166947005) Valproate level low (1153409008) Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) (1171357005) Vitamin B12 deficiency anemia following gastrectomy (disorder) (1153353002) Vitamin B12 deficiency anemia following total gastrectomy (disorder) (167846009) Vomit: excessive acidity (719019000) WT limb blood syndrome (disorder) (3978000) Warm autoimmune hemolytic anemia (165659002) Whole blood folate low (403837005) Wiskott-Aldrich autosomal dominant variant syndrome (disorder) (36070007) Wiskott-Aldrich syndrome (254131007) Worth disease (249916005) Wrist stiff (21412009) X chromosome-linked pyridoxine refractory sideroblastic anemia (25443007) X chromosome-linked pyridoxine responsive sideroblastic anemia (48983004) X chromosome-linked sideroblastic anemia (782786001) X-linked calvarial hyperostosis (771148008) X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder) (722475006) X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) (782759001) X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) (1197588008) X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) (782785002) X-linked osteoporosis with fractures (718882006) X-linked severe congenital neutropenia (disorder) (719816006) X-linked sideroblastic anemia with spinocerebellar ataxia (1156838007) X-linked thrombocytopenia with normal platelets (disorder) (68913001) alpha Thalassemia (36467003) alpha^+^ Thalassemia (86242003) alpha^+^ Thalassemia, deletion type (85422000) alpha^+^ Thalassemia, nondeletion type (66055002) alpha^0^ Thalassemia (65959000) beta Thalassemia (79592006) beta^+^ Thalassemia (47084006) beta^+^ Thalassemia, normal Hb A2, type 1, silent (15326009) beta^+^ Thalassemia, normal Hb A2, type 2 (86715000) beta^0^ Thalassemia (27080008) beta^0^ Thalassemia, deletion type (111572002) beta^0^ Thalassemia, nondeletion type (16427007) delta Thalassemia (16360009) delta beta Thalassemia (76336008) delta beta^0^ Thalassemia (62074008) delta^0^ Thalassemia (23371004) epsilon gamma delta beta Thalassemia (73190000) epsilon gamma delta beta^0^ Thalassemia
Child Concepts