OBO ID: DOID:0110842
Term Name: Usher syndrome type 3B Search Ontology:
Synonyms:
  • USH3B
  • Usher syndrome type IIIB
Definition: An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31. https://www.ncbi.nlm.nih.gov/pubmed/22279524
References:
Ontology: Human Disease   ( DOID:0110842 )
Relationships
is a type of:
inverse disjoint_from:
OTHER Usher syndrome type 3B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HARS Usher syndrome type 3B 614504
HARS2 Usher syndrome type 3B 614504
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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