OMOP Concept 36717145
Deaf blind hypopigmentation syndrome Yemenite type
StandardConditionSNOMED721084001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Deaf blind hypopigmentation syndrome Yemenite type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536771 | Yemenite deaf-blind hypopigmentation syndrome | Non-standard |
| Nebraska Lexicon | 721084001 | Deaf blind hypopigmentation syndrome Yemenite type | Non-standard |
Synonyms
Alternative names recorded for Deaf blind hypopigmentation syndrome Yemenite type across source vocabularies.
- Deaf blind hypopigmentation syndrome Yemenite type (disorder)
- síndrome de sordera, ceguera e hipopigmentación tipo yemenita
- síndrome de sordera, ceguera e hipopigmentación tipo yemenita (trastorno)
- síndrome de Warburg Thomsen
- Warburg Thomsen syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(59)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of eye
- 1Congenital deficiency of pigment of skin
- 1Developmental hereditary disorder
- 1Genetic disorder of skin pigmentation
- 1Hearing loss associated with syndrome
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 1Multiple system malformation syndrome
- 2Anomaly of eye
- 2Autosomal hereditary disorder
- 2Congenital anomaly of head
- 2Congenital anomaly of visual system
- 2Congenital malformation syndrome
- 2Congenital pigmentary skin anomalies
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of integument
- 2Disorder of skin pigmentation
- 2Genetic disease
- 2Hearing loss
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Skin hypopigmented
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