deafness, autosomal dominant 2A - CISMeF

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CISMeF

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Deafness, autosomal dominant 2AMeSH concept

Preferred Label : deafness, autosomal dominant 2A;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0567741;

UMLS CUI

C2677637;

Currated CISMeF NLP mapping
- Deafness, autosomal dominant 2a [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 2A [DO Concept]
Related record
- deafness, autosomal dominant 2A [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 2a [OMIM Phenotype]
- autosomal dominant nonsyndromic deafness 2A [DO Concept]

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25/05/2025

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