Deafness, autosomal recessive 51

Preferred Label : Deafness, autosomal recessive 51;

Symbol : DFNB51;

CISMeF acronym : DFNB51;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %609941;

Details

Origin ID

609941;

UMLS CUI

C1864968;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive non-syndromic sensorineural deafness type DFNB [ORDO Disease]
Currated CISMeF NLP mapping
- Deafness, autosomal recessive 51 [MeSH concept]
- autosomal recessive nonsyndromic deafness 51 [DO Concept]
- deafness, autosomal recessive 51 [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive nonsyndromic deafness 51 [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Bilateral sensorineural deafness [HPO term]
- Sensorineural deafness [HPO term]
- Sensorineural hearing impairment [HPO term]
ORDO concept(s)
- Autosomal recessive non-syndromic sensorineural deafness type DFNB [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 51 [MeSH concept]
- autosomal recessive nonsyndromic deafness 51 [DO Concept]
- deafness, autosomal recessive 51 [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients