OMOP Concept 4051702
Family history of congenital disease
StandardObservationSNOMED160417009Context-dependent
Maps from
15
Descendants
74
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Family history of congenital disease via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Family history of congenital disease across source vocabularies.
- antecedente familiar de anomalía congénita
- antecedente familiar de enfermedad congénita
- antecedente familiar de enfermedad congénita (situación)
- Family history of congenital anomaly
- Family history of congenital disease (situation)
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
(74)Included automatically when you query with descendants.
- 1Family history of 5,10 methylenetetrahydrofolate reductase deficiency
- 1Family history of alpha-1-antitrypsin deficiency
- 1Family history of chromosomal anomaly
- 1Family history of congenital immunodeficiency disease
- 1Family history of congenital malformation
- 1Family history of congenital sensorineural hearing loss
- 1Family history of glycogen storage disease
- 1Family history of hemoglobinopathy E
- 1Family history of lysosomal storage disease
- 1Family history of neurofibromatosis
- 1Family history of phenylketonuria
- 1Family history of sickle cell anemia
- 1Family history of tuberous sclerosis
- 1Family history of Von Hippel-Lindau syndrome
- 1FH: Polycystic kidney
- 1FH: Sickle cell trait
- 1FH: Thalassemia
- 1Mother of child with Mobius syndrome
- 1Mother of child with Turners syndrome
- 2Family history of alpha thalassemia
- 2Family history of anencephaly
- 2Family history of asplenia
- 2Family history of beta thalassemia
- 2Family history of cleft lip
- 2Family history of cleft palate
- 2Family history of complete trisomy 21 syndrome
- 2Family history of congenital anomaly of cardiovascular system
- 2Family history of congenital anomaly of ear
- 2Family history of congenital cataract
- 2Family history of congenital hydrocephalus
- 2Family history of congenital microcephaly
- 2Family history of cystic hygroma
- 2Family history of Downs syndrome
- 2Family history of dysmorphism
- 2Family history of fragile X syndrome
- 2Family history of fragile X syndrome in first degree relative
- 2Family history of gastroschisis
- 2Family history of multiple congenital anomalies
- 2Family history of sex chromosome aneuploidy
- 2Family history of sex chromosome translocation
- 2Family history of single congenital anomaly
- 2Family history of Tay-Sachs disease
- 2Family history of trisomy 13
- 2Family history of trisomy 18
- 2Family history of Turner syndrome
- 2Family history of velocardiofacial syndrome
- 2FH: Congenital GIT anomaly
- 2FH: Congenital GU anomaly
- 2FH: Congenital RS anomaly
- 2FH: Cong. orthopedic anomaly
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