OBO ID: DOID:0110832
Term Name: Usher syndrome type 1F Search Ontology:
Synonyms:
  • USH1F
  • Usher syndrome type IF
Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. https://www.ncbi.nlm.nih.gov/pubmed/11398101
References:
Ontology: Human Disease   (DOID:0110832)
OTHER Usher syndrome type 1F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PCDH15 Usher syndrome, type 1F 602083
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None