OMOP Concept 4051564
Family history of metabolic disorder
StandardObservationSNOMED160305008Context-dependent
Maps from
5
Descendants
42
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Family history of metabolic disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Z83.4 | Family history of other endocrine, nutritional and metabolic diseases | Non-standard |
| ICD10CM | Z83.49 | Family history of other endocrine, nutritional and metabolic diseases | Non-standard |
| Nebraska Lexicon | 160305008 | Family history of metabolic disorder | Non-standard |
| Read | 126..00 | FH: Metabolic disorder | Non-standard |
| Read | 126Z.00 | FH: Metabolic disorder NOS | Non-standard |
Synonyms
Alternative names recorded for Family history of metabolic disorder across source vocabularies.
- antecedente familiar de metabolopatía
- antecedente familiar de trastorno metabólico
- antecedente familiar de trastorno metabólico (situación)
- Family history: Metabolic disorder
- Family history of metabolic disorder (situation)
- FH: Metabolic disorder
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(42)Included automatically when you query with descendants.
- 1Family history of 5,10 methylenetetrahydrofolate reductase deficiency
- 1Family history of acetylcholinesterase deficiency
- 1Family history of alpha-1-antitrypsin deficiency
- 1Family history of butyrylcholinesterase deficiency
- 1Family history of Canavan disease
- 1Family history of diabetes mellitus
- 1Family history of galactosemia
- 1Family history of glycogen storage disease
- 1Family history of Graves disease
- 1Family history of hemochromatosis
- 1Family history of hyperbetalipoproteinemia
- 1Family history of hyperlipidemia
- 1Family history of hypoalphalipoproteinemia
- 1Family history of impaired glucose tolerance
- 1Family history of lipoprotein (a) hyperlipoproteinemia
- 1Family history of lysosomal storage disease
- 1Family history of methylmalonic aciduria
- 1Family history of mitochondrial disease
- 1Family history of phenylketonuria
- 1Family history of polycystic ovary syndrome
- 1Family history of thyrotoxicosis
- 1Family history of Wilson disease
- 1FH: Diabetes in pregnancy
- 1FH: Gout
- 1FH: MCADD (medium chain acyl coenzyme A dehydrogenase deficiency)
- 1FH: Porphyria
- 2Family history of combined hyperlipidemia
- 2Family history of diabetes mellitus in first degree relative
- 2Family history of diabetes mellitus type 1
- 2Family history of diabetes mellitus type 2
- 2Family history of hypertriglyceridemia
- 2Family history of Tay-Sachs disease
- 2FH: Hypercholesterolemia
- 2Maternal history of diabetes mellitus
- 2Maternal history of gestational diabetes
- 2Maternal history of Graves' disease
- 3Family history of familial hypercholesterolemia
- 3FH: Hypercholesterolemia in first degree relative
- 3Maternal history of diabetes mellitus type 1
- 3Maternal history of diabetes mellitus type 2
- 4Family history of double heterozygous familial hypercholesterolemia
- 4Family history of Fredrickson type IIa hyperlipoproteinemia
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