OBO ID: DOID:0080262
Term Name: autosomal recessive nonsyndromic deafness 107 Search Ontology:
Synonyms:
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in compound heterozygous mutation in the WBP2 gene on chromosome 17q25. https://pubmed.ncbi.nlm.nih.gov/26881968/
References:
Ontology: Human Disease   ( DOID:0080262 )
OTHER autosomal recessive nonsyndromic deafness 107 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WBP2 Deafness, autosomal recessive 107 617639
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None