deafness, autosomal recessive 22

Preferred Label : deafness, autosomal recessive 22;

MeSH note : mutation in OTOA;

MeSH synonym : DFNB22;

Origin ID

C564633;

UMLS CUI

C1846896;

Currated CISMeF NLP mapping
- Deafness, autosomal recessive 22 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 22 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive 22 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 22 [OMIM Phenotype]