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Concept IDs
SNOMEDCT
722206009
conceptId
722206009
fullName
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder)
preferred
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder)
acceptable
Yorifuji Okuno syndrome
preferredName
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder)
semanticTag
disorder
synonym
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
Yorifuji Okuno syndrome
description
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder)
Yorifuji Okuno syndrome
active
true
activeDate
Jan 31, 2017
effectiveDate
Jan 31, 2017
moduleId
900000000000207008
definitionStatusId
900000000000074008
associated morphology
(55199003) Hypoplasia (49755003) Morphologically abnormal structure
pathological process
(308490002) Pathological developmental process
finding site
(80891009) Heart structure (119218006) Pancreas part
finding site is-a
(818983003) Abdomen (818984009) Abdomen proper (818985005) Abdomen proper segment of trunk (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 (305072005) Breast and endocrine structures (113257007) Cardiovascular structure (281233007) Cardiovascular structure of trunk (416775004) Chest and/or abdomen and/or pelvis structure (body structure) (416550000) Chest and/or abdomen structure (body structure) (818981001) Cross-sectional abdomen (119210004) Digestive organ part (49596003) Digestive organ structure (86762007) Digestive structure (113331007) Endocrine structure (409708007) Heart AND pericardium structure (80891009) Heart structure (281501002) Intra-abdominal digestive structure (818988007) Intra-abdominal proper structure (818986006) Intra-abdominopelvic structure (281467004) Intrathoracic cardiovascular structure (69548008) Lower body part structure (128263001) Lower body structure (63337009) Lower trunk structure (310787001) Lung and mediastinal structures (72410000) Mediastinal structure (69608005) Middle mediastinum structure (416152001) Neck and/or chest and/or abdomen structure (body structure) (417437006) Neck and/or chest structure (body structure) (416319003) Neck, chest, abdomen, and pelvis (91717005) Organ part (119218006) Pancreas part (15776009) Pancreatic structure (280432007) Region of mediastinum (281827007) Regional cardiovascular structure (82849001) Retroperitoneal compartment structure (body structure) (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 (699593001) Structure of compartment of thorax (1187376008) Structure of inferior mediastinum (body structure) (818993005) Structure of organ within abdominopelvic cavity (body structure) (420473002) Structure of subregion of trunk (body structure) (816094009) Structure of thoracic cross-sectional segment of trunk (body structure) (27832009) Structure of thoracic viscus (362937008) Structure of viscus (699602007) Structure of viscus of abdomen proper (243951005) Subdivision of inferior mediastinum (51185008) Thoracic structure (22943007) Trunk structure (70104002) Upper body part structure (128262006) Upper body structure (67734004) Upper trunk structure
associated morphology is-a
(123037004) Body structure (57697001) Growth alteration (55199003) Hypoplasia (41010001) Maturation defect (49755003) Morphologically abnormal structure (118956008) Morphologically altered structure (138875005) SNOMED CT Concept
occurrence
(255399007) Congenital
occurrence is-a
(255399007) Congenital (272099008) Descriptor (qualifier value) (282032007) Periods of life (703763000) Precondition value (qualifier value) (362981000) Qualifier value (138875005) SNOMED CT Concept (281586009) Special atomic mapping values (303102005) Special disorder atoms (307142001) Temporal periods (272103003) Time patterns
pathological process is-a
(308490002) Pathological developmental process (308489006) Pathological process (719982003) Process (qualifier value) (362981000) Qualifier value (138875005) SNOMED CT Concept (281586009) Special atomic mapping values (303102005) Special disorder atoms
Child Concepts
Parent Concepts
(11164009) Autosomal dominant hereditary disorder (13213009) Congenital heart disease (363104002) Hereditary disorder of endocrine system (disorder) (73211009) Diabetes mellitus (363070008) Developmental hereditary disorder (363005004) Cardiovascular system hereditary disorder (363080007) Digestive system hereditary disorder (68591005) Congenital hypoplasia of pancreas