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Concept IDs
SNOMEDCT
160305008
conceptId
160305008
fullName
Family history of metabolic disorder (situation)
preferred
Family history of metabolic disorder
Family history of metabolic disorder (situation)
FH: Metabolic disorder
acceptable
Family history: Metabolic disorder
FH: Metabolic disorder
preferredName
FH: Metabolic disorder
semanticTag
context-dependent category
situation
synonym
Family history: Metabolic disorder
Family history of metabolic disorder
FH: Metabolic disorder
description
Family history: Metabolic disorder
Family history of metabolic disorder
Family history: Metabolic disorder (situation)
Family history: Metabolic disorder (context-dependent category)
Family history of metabolic disorder (situation)
FH: Metabolic disorder
active
true
activeDate
Jul 31, 2004
Jan 31, 2002
effectiveDate
Jan 31, 2002
moduleId
900000000000207008
definitionStatusId
900000000000074008
subject relationship context
(444148008) Person in family of subject (person)
subject relationship context is-a
(125676002) Person (444148008) Person in family of subject (person) (303071001) Person in the family (person) (444018008) Person with characteristic related to subject of record (person) (138875005) SNOMED CT Concept (48176007) Social context
finding context is-a
(288529006) Context values (410514004) Finding context value (qualifier value) (36692007) Known (410515003) Known present (qualifier value) (362981000) Qualifier value (138875005) SNOMED CT Concept
temporal context
(410511007) Current or past (actual) (qualifier value)
finding context
(410515003) Known present (qualifier value)
associated finding
(75934005) Metabolic disease
associated finding is-a
(404684003) Clinical finding (finding) (64572001) Disease (75934005) Metabolic disease (138875005) SNOMED CT Concept
temporal context is-a
(288529006) Context values (410511007) Current or past (actual) (qualifier value) (362981000) Qualifier value (138875005) SNOMED CT Concept (410510008) Temporal context value (qualifier value)
Child Concepts
(699108005) Family history of tendinous xanthoma in first degree relative (789240000) Family history of acetylcholinesterase deficiency (29810001000004100) Family history of 5,10 methylenetetrahydrofolate reductase deficiency (situation) (160310007) FH: Porphyria (74171000119103) Family history of hypoalphalipoproteinemia (situation) (160308005) FH: Gout (64081000119105) Family history of galactosemia (109241000119103) Family history of eruptive xanthoma (situation) (431912005) Family history of alpha-1-antitrypsin deficiency (situation) (160402005) FH: Diabetes in pregnancy (456561000124100) Family history of Wilson disease (situation) (74131000119101) Family history of hyperbetalipoproteinemia (situation) (781073000) Family history of polycystic ovary syndrome (64131000119105) Family history of methylmalonic aciduria (situation) (160303001) FH: Diabetes mellitus (64161000119102) Family history of phenylketonuria (63901000119104) Family history of Tay-Sachs disease (109231000119107) Family history of xanthelasma (situation) (98011000119108) Family history of pseudocholinesterase deficiency (7310001000004107) Family history of Graves disease (situation) (98251000119101) Family history of Canavan disease (473070008) Family history of mitochondrial disease (401119001) Family history of hemochromatosis (situation) (725117008) Family history of hyperlipidemia (situation) (109261000119104) Family history of tuberous xanthoma (situation) (699109002) Family history of tendinous xanthoma in second degree relative (situation) (64251000119106) Family history of glycogen storage disease (situation) (429971003) Family history of impaired glucose tolerance (situation)
Parent Concepts
(281666001) Family history of disorder