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Metadata
ID DOID:0110842
Name Usher syndrome type 3B
Definition An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31.
https://www.ncbi.nlm.nih.gov/pubmed/22279524
Xrefs

ICD10CM:H35.5

OMIM:614504

Synonyms

USH3B [EXACT]

Usher syndrome type IIIB [EXACT]

Parent Relationships

is_a Usher syndrome type 3

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