Search Ontology:
Human Disease

Usher syndrome type 1F

Term ID
DOID:0110832
Synonyms
  • USH1F
  • Usher syndrome type IF
Definition
An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. https://www.ncbi.nlm.nih.gov/pubmed/11398101
References
Ontology
Human Disease   ( DOID:0110832 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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