Search Ontology:
Human Disease

Usher syndrome type 2C

Term ID
DOID:0110839
Synonyms
  • USH2C
  • Usher syndrome IIC
  • Usher syndrome type IIC
Definition
An Usher syndrome type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14. https://www.ncbi.nlm.nih.gov/pubmed/14740321
References
Ontology
Human Disease   ( DOID:0110839 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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