OMOP Concept 4007235
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
StandardConditionSNOMED10170007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Black locks, oculocutaneous albinism, AND deafness of the sensorineural type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 147262 | Black locks, oculocutaneous albinism, and deafness of the sensorineural type | Non-standard |
| MeSH | C562663 | BADS Syndrome | Non-standard |
Synonyms
Alternative names recorded for Black locks, oculocutaneous albinism, AND deafness of the sensorineural type across source vocabularies.
- BADS syndrome
- Black locks, oculocutaneous albinism, AND deafness of the sensorineural type (disorder)
- mechones oscuros, albinismo oculocutáneo Y sordera de tipo neurosensorial
- mechones oscuros, albinismo oculocutáneo Y sordera de tipo neurosensorial (trastorno)
- síndrome BADS (black locks, oculocutaneous albinism, AND deafness of the sensorineural type) - mechones oscuros, albinismo oculocutáneo Y sordera de tipo neurosensorial
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(68)Roll up to these when you need a wider cohort.
- 1Congenital sensorineural hearing loss
- 1Hearing loss associated with syndrome
- 1Hereditary hearing loss
- 1Oculocutaneous albinism
- 2Albinism
- 2Auditory system hereditary disorder
- 2Autosomal recessive hereditary disorder
- 2Congenital hearing disorder
- 2Congenital oculocutaneous hypopigmentation
- 2Genetic disorder of skin pigmentation
- 2Hearing loss
- 2Hereditary disorder of the integument
- 2Hereditary disorder of the visual system
- 2Sensorineural hearing loss
- 3Autosomal hereditary disorder
- 3Congenital anomaly of eye
- 3Congenital deficiency of pigment of skin
- 3Congenital disease
- 3Congenital malformation
- 3Developmental hereditary disorder
- 3Disorder of auditory system
- 3Disorder of integument
- 3Disorder of pigmentation
- 3Disorder of skin pigmentation
- 3Genetic disease
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