OMOP Concept 4209750
Congenital hypertrichosis
StandardConditionSNOMED56797000Disorder
Maps from
3
Descendants
12
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Congenital hypertrichosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143915 | Congenital hypertrichosis | Non-standard |
| Nebraska Lexicon | 56797000 | Congenital hypertrichosis | Non-standard |
| Read | PH42.00 | Congenital hypertrichosis | Non-standard |
Synonyms
Alternative names recorded for Congenital hypertrichosis across source vocabularies.
- Congenital hypertrichosis (disorder)
- hipertricosis congénita
- hipertricosis congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of hair
- 1Hypertrichosis
- 2Congenital anomaly of skin
- 2Disorder of hair
- 2Disorder of hair growth
- 3Congenital anomaly of integument
- 3Disorder of skin
- 3Disorder of skin appendage
- 3Hair finding
- 4Congenital malformation
- 4Disorder involving the integument of fetus OR newborn
- 4Disorder of skin and/or subcutaneous tissue
- 4Skin finding
- 5Congenital disease
- 5Developmental disorder
- 5Disorder of fetus and/or newborn
- 5Disorder of integument
- 5Disorder of soft tissue
- 5General finding of soft tissue
- 5Integumentary system finding
- 5Skin AND/OR mucosa finding
- 6Clinical finding
- 6Disease
- 6Disorder of body system
Narrower concepts
(12)Included automatically when you query with descendants.
- 1Amaurosis hypertrichosis syndrome
- 1Barber-Say syndrome
- 1Cervical hypertrichosis and peripheral neuropathy syndrome
- 1Congenital cataract with hypertrichosis and intellectual disability syndrome
- 1Congenital generalized hypertrichosis
- 1Congenital hypertrichosis lanuginosa
- 1Hypertrichosis cubiti
- 1Hypertrichosis with congenital macrogingivae
- 1Isolated anterior cervical hypertrichosis
- 1Wiedemann Steiner syndrome
- 2Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome
- 2X-linked congenital generalized hypertrichosis
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