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91689009: Body system structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

32409 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Body system structure Is a Anatomical structure true Inferred relationship Existential restriction modifier (core metadata concept)
Body system structure partie de Entire body as a whole (body structure) false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Cytosine diphosphate choline phosphotransferase deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Dihydropyrimidinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Dihydropyrimidine dehydrogenase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of lipid storage and metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Sphingolipidosis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Galactocerebroside beta-galactosidase deficiency - early onset (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Arylsulfatase A deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of cholesterol catabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
An anomaly of bile acid synthesis with characteristics of severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins. Patients present with neonatal cholestasis and rapid progression to cirrhosis and death in infancy without intervention. Caused by a mutation in the delta(4)-3-oxosteroid 5-beta-reductase gene (AKR1D1, 7q32-q33). Transmission is autosomal recessive. Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of cholesterol synthesis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of lipoprotein storage and metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial combined hyperlipidemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of glycosaminoglycan metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of glycoprotein metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Carbohydrate-deficient glycoprotein syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of sialic acid metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Sialuria (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of porphyrin and hem metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous erythropoietic protoporphyria Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous acute intermittent porphyria Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of peroxisomal function Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
General loss of peroxisomal function (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Infantile Refsum's disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Loss of multiple peroxisomal functions (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Zellweger's-like syndrome (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Pseudoinfantile Refsum's disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Loss of single peroxisomal function (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Peroxisomal thiolase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Bifunctional peroxisomal enzyme deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Glutaryl-coenzyme A oxidase deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Isolated dihydroxyacetone phosphate acyltransferase deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Isolated alkyldihydroxyacetone phosphate synthase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypercholesterolemia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Polygenic hypercholesterolaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypercholesterolaemia - homozygous Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypercholesterolaemia - heterozygous Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hyperalphalipoproteinemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial defective apolipoprotein B-100 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Secondary hypercholesterolemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypertriglyceridaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Fredrickson type IV hyperlipoproteinemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
hyperlipoprotéinémie de Fredrickson type I Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Secondary hypertriglyceridemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Primary combined hyperlipidemia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Secondary combined hyperlipidemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hypolipidemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypobetalipoproteinemia - homozygous form (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypobetalipoproteinaemia - heterozygous form Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apolipoprotein A-I deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apolipoprotein A-I variant disorder Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apo A-I Milano variant Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apo A-I Marburg variant (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 1 (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 2 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
ApoA-I Munster variant 3 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apo A-I Giessen variant Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Apo A-I variant fisheye-like syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Sitosterolemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Sodium deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Chloride deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Calcium deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Magnesium deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Phosphate deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Trace element deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Iodine deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Molybdenum deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Vanadium deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Zinc deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Infantile beriberi (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Pantothenic acid deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hypervitaminosis B6 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of blood gas (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hyperoxia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of oxygen transport (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Impaired oxygen delivery Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Impaired oxygen extraction Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Increased oxygen demand (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Neurological mental status determination Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Slocum's test Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Crossed straight leg test Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Anterior drawer test Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinman test (procedure) Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Secondary gout (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Gout secondary to renal impairment (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Gout secondary to drug Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Gout caused by lead (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Gout secondary to enzyme defect Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Abduction test of knee (procedure) Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Glasgow coma testing and evaluation Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Spurling manoeuvre Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Metabolic acidosis, normal anion gap (NAG) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Mineral deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Chemically-induced lipidosis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Porphyria caused by toxic effect of substance (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Localized amyloid deposit Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Metabolic disorder of transport (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Saccharopinuria Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Vitamin A deficiency with ocular manifestation (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohyperparathyroidism Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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