deafness, autosomal recessive

Preferred Label : deafness, autosomal recessive;

Origin ID

C564609;

UMLS CUI

C1846647;

Automatic exact mappings (from CISMeF team)
- Gap junction protein, beta-3 [OMIM Phenotype]
CISMeF manual mappings
- autosomal recessive non syndromic sensorineural deafness [Disease (Nov.)]
Currated CISMeF NLP mapping
- Deafness, autosomal recessive [OMIM phenotypic series]
- Deafness, autosomal recessive [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive [MeSH 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]