deafness, autosomal recessive 49

Preferred Label : deafness, autosomal recessive 49;

MeSH synonym : DFNB49;

Origin ID

C565717;

UMLS CUI

C1857811;

Currated CISMeF NLP mapping
- Deafness, Autosomal Recessive 49 [NCIt concept]
- Deafness, autosomal recessive 49 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 49 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive 49 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, Autosomal Recessive 49 [NCIt concept]
- Deafness, autosomal recessive 49 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 49 [DO Concept]