deafness, autosomal recessive 1A

Preferred Label : deafness, autosomal recessive 1A;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567434;

UMLS CUI

C2673759;

Currated CISMeF NLP mapping
- Deafness, Autosomal Recessive 1A [NCIt concept]
- Deafness, autosomal recessive 1a [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 1A [DO Concept]
Related MeSH concept(s)
- deafness, digenic, Gjb2-Gjb3 [MeSH concept]
- deafness, digenic, Gjb2-Gjb6 [MeSH concept]
Related record
- deafness, autosomal recessive 1A [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, Autosomal Recessive 1A [NCIt concept]
- Deafness, autosomal recessive 1a [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 1A [DO Concept]