OBO ID: DOID:0110491
Term Name: autosomal recessive nonsyndromic deafness 32 Search Ontology:
Synonyms:
  • autosomal recessive deafness 32
  • DFNB32
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in variation in the chromosome region 1p22.1-p13.3.https://www.ncbi.nlm.nih.gov/pubmed/12634867
References:
Ontology: Human Disease   (DOID:0110491)
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 32 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDC14A Deafness, autosomal recessive 32, with or without immotile sperm 608653
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None