OBO ID: DOID:0110519
Term Name: autosomal recessive nonsyndromic deafness 68 Search Ontology:
Synonyms:
  • autosomal recessive deafness 68
  • DFNB68
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13.https://www.ncbi.nlm.nih.gov/pubmed/26805784
References:
Ontology: Human Disease   (DOID:0110519)
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 68 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
S1PR2 Deafness, autosomal recessive 68 610419
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None