Search Ontology:
Human Disease

Usher syndrome type 2D

Term ID
DOID:0110840
Synonyms
  • USH2D
  • Usher syndrome type IID
Definition
An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/17171570
References
  • ICD10CM:H35.5
  • MIM:611383
Ontology
Human Disease   ( DOID:0110840 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations