Deafness, autosomal dominant 52

Preferred Label : Deafness, autosomal dominant 52;

Obsolete resource : true;

Moved to : 602459;

Symbol : DFNA52;

CISMeF acronym : DFNA42; DFNA52;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Deafness, autosomal dominant 42; DFNA42;

Inheritance : Autosomal dominant;

Prefixed ID : 607683;

Details

Origin ID

607683;

UMLS CUI

C1843232;

Currated CISMeF NLP mapping
- autosomal dominant nonsyndromic deafness 52 [DO Concept]
- deafness, autosomal dominant 52 [MeSH concept]
- deafness, autosomal dominant 52 [MeSH Supplementary Concept]
DO Cross reference
- autosomal dominant nonsyndromic deafness 52 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hearing impairment [HPO term]
ORDO concept(s)
- Autosomal dominant non-syndromic sensorineural deafness type DFNA [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- autosomal dominant nonsyndromic deafness 52 [DO Concept]
- deafness, autosomal dominant 52 [MeSH Supplementary Concept]
- deafness, autosomal dominant 52 [MeSH concept]

Keyword's position in hierarchy(ies) :

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