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Metadata
ID DOID:0110834
Name Usher syndrome type 1G
Definition An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.
https://www.ncbi.nlm.nih.gov/pubmed/12588794
Xrefs

ICD10CM:H35.5

OMIM:606943

Synonyms

USH1G [EXACT]

Usher syndrome type IG [EXACT]

Parent Relationships

is_a Usher syndrome type 1

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