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Metadata
DOID DOID:0110840
Name Usher syndrome type 2D
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
Synonyms

USH2D [EXACT]

Usher syndrome type IID [EXACT]

Xrefs

ICD10CM:H35.5

OMIM:611383

Relationships

is_a Usher syndrome type 2

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