OBO ID: DOID:0080263
Term Name: autosomal recessive nonsyndromic deafness 108 Search Ontology:
Synonyms:
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the ROR1 gene on chromosome 1p31. https://pubmed.ncbi.nlm.nih.gov/27162350/
References:
Ontology: Human Disease   ( DOID:0080263 )
OTHER autosomal recessive nonsyndromic deafness 108 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ROR1 ?Deafness, autosomal recessive 108 617654
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None