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Human Disease

autosomal recessive nonsyndromic deafness 111

Term ID
DOID:0111640
Synonyms
  • 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 )
Relationships
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Genes Involved
Zebrafish Models