deafness, autosomal recessive 9

Preferred Label : deafness, autosomal recessive 9;

MeSH note : mutationin otoferlin;

MeSH synonym : auditory neuropathy, autosomal recessive, 1; neurosensory nonsyndromic recessive deafness 9;

Details

Origin ID

C563396;

UMLS CUI

C1832828;

Currated CISMeF NLP mapping
- Deafness, autosomal recessive 9 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 9 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive 9 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 9 [OMIM Phenotype]

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