OMOP Concept 4136453
Family history of development disorder
StandardObservationSNOMED412749001Context-dependent
Maps from
2
Descendants
59
Valid from
31 Jul 2004
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Family history of development disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 412749001 | Family history of development disorder | Non-standard |
| Read | 12W..00 | Family history of development disorder | Non-standard |
Synonyms
Alternative names recorded for Family history of development disorder across source vocabularies.
- antecedente familiar de trastorno del desarrollo
- antecedente familiar de trastorno del desarrollo (situación)
- Family history of development disorder (situation)
- FH: Development 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
(59)Included automatically when you query with descendants.
- 1Family history of attention deficit hyperactivity disorder
- 1Family history of autism
- 1Family history of congenital malformation
- 1Family history of intellectual disability
- 1Family history of learning disability
- 1Family history of neurological developmental delay
- 1Family history of short stature
- 1FH: Muscular dystrophy
- 2Family history of achondroplasia
- 2Family history of anencephaly
- 2Family history of asplenia
- 2Family history of attention deficit hyperactivity disorder, predominantly inattentive type
- 2Family history of autism in sibling
- 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 dysmorphism
- 2Family history of fragile X syndrome
- 2Family history of gastroschisis
- 2Family history of multiple congenital anomalies
- 2Family history of myotonic dystrophy
- 2Family history of Rett syndrome
- 2Family history of single congenital anomaly
- 2Family history of Steinert myotonic dystrophy
- 2Family history of trisomy 18
- 2Father with learning disability
- 2FH: Congenital GIT anomaly
- 2FH: Congenital GU anomaly
- 2FH: Congenital RS anomaly
- 2FH: Cong. orthopedic anomaly
- 2Maternal learning disability
- 3Family history of ambiguous genitalia
- 3Family history of cleft palate with cleft lip
- 3Family history of congenital diaphragmatic hernia
- 3Family history of congenital Finnish nephrotic syndrome
- 3Family history of congenital hip dysplasia
- 3Family history of Cowden syndrome
- 3Family history of craniosynostosis
- 3Family history of holoprosencephaly
- 3Family history of hypospadias
- 3Family history of osteogenesis imperfecta
- 3Family history of Prader-Willi syndrome
- 3Family history of Spina bifida
- 3Family history of trisomy 18 syndrome
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