OBO ID: DOID:0110462
Term Name: autosomal recessive nonsyndromic deafness 101 Search Ontology:
Synonyms:
  • autosomal recessive deafness 101
  • DFNB101
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/24619944
References:
Ontology: Human Disease   ( DOID:0110462 )
OTHER autosomal recessive nonsyndromic deafness 101 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRXCR2 ?Deafness, autosomal recessive 101
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None