OBO ID: DOID:0110841
Term Name: Usher syndrome type 3A Search Ontology:
Synonyms:
  • USH3A
  • Usher syndrome type IIIA
Definition: An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25. https://www.ncbi.nlm.nih.gov/pubmed/11524702
References:
Ontology: Human Disease   ( DOID:0110841 )
Relationships
is a type of:
disjoint_from:
OTHER Usher syndrome type 3A PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLRN1 Usher syndrome, type 3A 276902
ZEBRAFISH MODELS
Fish Conditions Citations
clrn1cwr1003/cwr1003; cwr1006Tg standard conditions Gopal et al., 2019
PHENOTYPE No data available

CITATIONS (1)
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