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Human Disease
autosomal recessive nonsyndromic deafness 111
- Term ID
- DOID:0111640
- Synonyms
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- autosomal recessive deafness 111
- DFNB111
- Definition
- An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in the MPZL2 gene on chromosome 11q23.33. (2)
- References
- Ontology
- Human Disease ( DOID:0111640 )
- is a type of
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Genes Involved
Zebrafish Models