OMOP Concept 4331069
Family history of hereditary disease
StandardObservationSNOMED429962007Context-dependent
Maps from
3
Descendants
41
Valid from
31 Jul 2008
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Family history of hereditary disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117583 | Hereditary Disease in Family Possibly Affecting Fetus, Affecting Management of Mother, with Delivery | Non-standard |
| CIEL | 152469 | Family History of Genetic Disorder | Non-standard |
| Nebraska Lexicon | 429962007 | Family history of heritable disorder | Non-standard |
Synonyms
Alternative names recorded for Family history of hereditary disease across source vocabularies.
- antecedente familiar de enfermedad genética
- antecedente familiar de enfermedad hereditaria
- antecedente familiar de enfermedad hereditaria (situación)
- Family history of genetic disease
- Family history of hereditary disease (situation)
- Family history of heritable 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
(41)Included automatically when you query with descendants.
- 1Family history of 5,10 methylenetetrahydrofolate reductase deficiency
- 1Family history of achondroplasia
- 1Family history of alpha-1-antitrypsin deficiency
- 1Family history of Canavan disease
- 1Family history of Charcot-Marie-Tooth disease
- 1Family history of congenital Finnish nephrotic syndrome
- 1Family history of congenital long QT syndrome
- 1Family history of Cowden syndrome
- 1Family history of cystic fibrosis
- 1Family history of disorder due to sex chromosome abnormality
- 1Family history of double heterozygous familial hypercholesterolemia
- 1Family history of Factor V Leiden mutation
- 1Family history of familial dysautonomia
- 1Family history of familial multiple polyposis syndrome
- 1Family history of glycogen storage disease
- 1Family history of hemoglobinopathy E
- 1Family history of hereditary diffuse gastric cancer
- 1Family history of hereditary nonpolyposis colon cancer
- 1Family history of heritable malignancy
- 1Family history of lysosomal storage disease
- 1Family history of Marfan syndrome
- 1Family history of phenylketonuria
- 1Family history of protein C resistance
- 1Family history of retinitis pigmentosa
- 1Family history of sickle cell anemia
- 1Family history of spinocerebellar ataxia
- 1Family history of Steinert myotonic dystrophy
- 1Family history of tuberous sclerosis
- 1Family history of Von Hippel-Lindau syndrome
- 1Family history of Wilson disease
- 1FH: Hereditary spherocytosis
- 1FH: Huntington's chorea
- 1FH: Sickle cell trait
- 1FH: Thalassemia
- 2Family history of alpha thalassemia
- 2Family history of beta thalassemia
- 2Family history of fragile X syndrome
- 2Family history of hemophilia A
- 2Family history of Rett syndrome
- 2Family history of Tay-Sachs disease
- 2FH: Spherocytosis
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