Deafness, autosomal dominant 47

Preferred Label : Deafness, autosomal dominant 47;

Symbol : DFNA47;

CISMeF acronym : DFNA47;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %608652;

Details

Origin ID

608652;

UMLS CUI

C1837609;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant non-syndromic sensorineural deafness type DFNA [ORDO Disease]
Currated CISMeF NLP mapping
- autosomal dominant nonsyndromic deafness 47 [DO Concept]
- deafness, autosomal dominant 47 [MeSH concept]
- deafness, autosomal dominant 47 [MeSH Supplementary Concept]
DO Cross reference
- autosomal dominant nonsyndromic deafness 47 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Sensorineural 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 47 [DO Concept]
- deafness, autosomal dominant 47 [MeSH Supplementary Concept]
- deafness, autosomal dominant 47 [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients