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Metadata
ID DOID:0110360
Name retinitis pigmentosa 39
Definition A retinitis pigmentosa that has_material_basis_in mutation in the USH2A gene on chromosome 1q41.
https://www.ncbi.nlm.nih.gov/pubmed/12427073
Xrefs

ICD10CM:H35.5

OMIM:613809

Synonyms

RP39 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

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