Search Ontology:
Human Disease

Usher syndrome type 3A

Term ID
DOID:0110841
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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