deafness, autosomal recessive

Preferred Label : deafness, autosomal recessive;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0564909;

UMLS CUI

C1846647;

Automatic exact mappings (from CISMeF team)
- Gap junction protein, beta-3 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Deafness, autosomal recessive [OMIM phenotypic series]
- Deafness, autosomal recessive [OMIM Phenotype]
- autosomal recessive non syndromic sensorineural deafness [Disease (Nov.)]
- autosomal recessive nonsyndromic deafness [DO Concept]
Related record
- deafness, autosomal recessive [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive [OMIM Phenotype]
- autosomal recessive non syndromic sensorineural deafness [Disease (Nov.)]
- autosomal recessive nonsyndromic deafness [DO Concept]