OBO ID: DOID:0110831
Term Name: Usher syndrome type 1D Search Ontology:
Synonyms:
  • USH1D
  • Usher syndrome type ID
Definition: An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/11138009
References:
Ontology: Human Disease   ( DOID:0110831 )
Relationships
is a type of:
OTHER Usher syndrome type 1D PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDH23 Usher syndrome, type 1D 601067
Usher syndrome, type 1D/F digenic 601067
PCDH15 Usher syndrome, type 1D/F digenic 601067
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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