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Concept IDs
SNOMEDCT
85919009
conceptId
85919009
fullName
Disorder of intestine (disorder)
preferred
Disorder of intestine
Disorder of intestine (disorder)
acceptable
Disorder of intestine
Enteropathy
Intestinal disease
preferredName
Disorder of intestine
semanticTag
disorder
synonym
Disorder of intestine
Disease of intestine
Enteropathy
Intestinal disease
description
Disorder of intestine
Disorder of intestine (disorder)
Disease of intestine (disorder)
Disease of intestine
Enteropathy
Intestinal disease
active
true
activeDate
Jan 31, 2002
effectiveDate
Jan 31, 2002
moduleId
900000000000207008
definitionStatusId
900000000000073002
due to
(717946000) Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease (disorder)
finding site
(113276009) Intestinal structure
finding site is-a
(818983003) Abdomen
(442083009) Anatomical or acquired body structure (body structure)
(91723000) Anatomical structure
(113343008) Body organ structure
(38866009) Body part structure
(52530000) Body region structure
(123037004) Body structure
(91689009) Body system structure
(416775004) Chest and/or abdomen and/or pelvis structure (body structure)
(119210004) Digestive organ part
(49596003) Digestive organ structure
(86762007) Digestive structure
(709519000) Digestive tract part (body structure)
(51289009) Digestive tract structure
(122865005) Gastrointestinal tract structure
(113276009) Intestinal structure
(281501002) Intra-abdominal digestive structure
(818986006) Intra-abdominopelvic structure
(69548008) Lower body part structure
(128263001) Lower body structure
(372198002) Lower gastrointestinal tract part (body structure)
(5668004) Lower gastrointestinal tract structure
(63337009) Lower trunk structure
(91717005) Organ part
(138875005) SNOMED CT Concept
(818982008) Structure of abdominopelvic cross-sectional segment of trunk (body structure)
(699589007) Structure of anatomical cluster (body structure)
(699590003) Structure of anatomical compartment (body structure)
(91829005) Structure of body compartment
(786857006) Structure of intestine and/or mesentery (body structure)
(818993005) Structure of organ within abdominopelvic cavity (body structure)
(420473002) Structure of subregion of trunk (body structure)
(362937008) Structure of viscus
(22943007) Trunk structure
due to is-a
(271737000) Anemia
(105599000) Anemia related to disturbed DNA synthesis
(404684003) Clinical finding (finding)
(64572001) Disease
(414022008) Disorder of cellular component of blood (disorder)
(299691001) Finding of blood, lymphatics and immune system
(83414005) Macrocytic anemia
(53165003) Megaloblastic anemia
(49472006) Megaloblastic anemia due to vitamin B12 deficiency
(717946000) Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease (disorder)
(66612000) Nutritional anemia
(363246002) Nutritional deficiency associated condition
(138875005) SNOMED CT Concept
Child Concepts
(439013004) Stricture of anastomosis of intestine (disorder)
(78625002) Hyperparathyroidism due to intestinal malabsorption
(119522002) Disorder of small intestine
(370486009) Intestinal entrapment (disorder)
(81060008) Intestinal obstruction
(82380002) Foreign body in intestine
(17440005) Anal spasm
(62851005) Impaction of intestine
(396331005) Celiac disease (disorder)
(45299002) Intestinal autonomic neuropathy
(235832002) Hollow visceral neuropathy
(370472005) Intestinal smooth muscle hypertrophy (disorder)
(22169002) Intestinal disaccharidase deficiency
(126769007) Neoplasm of intestinal tract
(737557007) Intestinal angioedema caused by angiotensin-converting enzyme inhibitor (disorder)
(128333008) Diarrheal disorder
(81120009) Functional disorder of intestine
(119523007) Disorder of large intestine
(235594008) Bowel dysfunction
(266071000) Intestinal infectious disease
(425671009) Neurogenic bowel (disorder)
(76341000) Koenig's syndrome II
(29886007) Adhesion of intestine
(28212002) Intestinal lipofuscinosis
(23065003) Stenosis of intestine
(700425005) Non-steroidal anti-inflammatory drug-induced enteropathy
(24754009) Isolated familial intestinal hypomagnesemia
(85942002) Ulceration of intestine
(59253004) Catarrhal dysentery
(126764002) Congenital anomaly of intestinal tract
(712510007) Intestinal hemorrhage (disorder)
(397881000) Diverticular disease (disorder)
(12851000119104) Dieulafoy's vascular malformation of intestine (disorder)
(141001000119104) Milk protein enteropathy (disorder)
(76641005) Prolapse of intestine
(24557004) Abscess of intestine
(49286008) Strangulation of intestine
(254588001) Polyp of intestine
(38851006) Fistula of intestine
(237575002) Abnormality of vasoactive intestinal peptide secretion
(17465007) Pneumatosis cystoides intestinalis
(254594009) Hamartoma of intestine
(40775003) Intestinal hernia
(675003) Torsion of intestine
(153821000119103) Visceral ischemia
(40515007) Concretion of intestine
(763630007) Satoyoshi syndrome
(56661000) Intestinal enteropeptidase deficiency
(38032004) Nonpersistence of intestinal lactase
(5562006) Endometriosis of intestine
(49723003) Intussusception of intestine
(22542007) Exudative enteropathy
(13160009) Complication of transplanted intestines
(125625000) Injury of intestine
(1187638005) Inflammation of intestine (disorder)
(77147000) Malabsorption in the elderly
(254595005) Nodular lymphoid hyperplasia of intestine
(86247009) Dilatation of intestine
Parent Concepts
(249562008) Bowel finding
(76712006) Disorder of digestive organ (disorder)
(79787007) Disorder of lower gastrointestinal tract (disorder)