OBO ID: DOID:0110834
Term Name: Usher syndrome type 1G Search Ontology:
Synonyms:
  • USH1G
  • Usher syndrome type IG
Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/12588794
References:
Ontology: Human Disease   ( DOID:0110834 )
Relationships
is a type of:
OTHER Usher syndrome type 1G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
USH1G Usher syndrome, type 1G 606943
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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