OBO ID: DOID:0110836
Term Name: Usher syndrome type 1J Search Ontology:
Synonyms:
  • USH1J
  • Usher syndrome type IJ
Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous mutation in the CIB2 gene on chromosome 15q24. https://www.ncbi.nlm.nih.gov/pubmed/23023331
References:
Ontology: Human Disease   ( DOID:0110836 )
Relationships
is a type of:
OTHER Usher syndrome type 1J PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CIB2 Usher syndrome, type IJ 614869
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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