OBO ID: DOID:0111640
Term Name: autosomal recessive nonsyndromic deafness 111 Search Ontology:
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
is a type of:
OTHER autosomal recessive nonsyndromic deafness 111 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MPZL2 Deafness, autosomal recessive 111 618145
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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