deafness, Childhood-Onset neurosensory, autosomal recessive 8

Preferred Label : deafness, Childhood-Onset neurosensory, autosomal recessive 8;

MeSH note : mutation in TMPRSS3;

MeSH synonym : neurosensory nonsyndromic recessive deafness 8;

Details

Origin ID

C563395;

UMLS CUI

C1832827;

Currated CISMeF NLP mapping
- Deafness, autosomal recessive 8 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 8 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, Childhood-Onset neurosensory, autosomal recessive 8 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 8 [OMIM Phenotype]

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