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 )
Relationships
is a type of:
OTHER Usher syndrome type 1F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PCDH15 Usher syndrome, type 1F 602083
PHENOTYPE No data available

CITATIONS (1)
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