Search Ontology:
Human Disease

Usher syndrome type 1D

Term ID
DOID:0110831
Synonyms
  • USH1D
  • Usher syndrome type ID
Definition
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/11138009
References
Ontology
Human Disease   ( DOID:0110831 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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