OBO ID: DOID:0110840
Term Name: Usher syndrome type 2D Search Ontology:
Synonyms:
  • USH2D
  • Usher syndrome type IID
Definition: An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/17171570
References:
Ontology: Human Disease   (DOID:0110840)
OTHER Usher syndrome type 2D PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WHRN Usher syndrome, type 2D 611383
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None