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Metadata
ID DOID:0110366
Name retinitis pigmentosa 33
Definition A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.
https://www.ncbi.nlm.nih.gov/pubmed/19878916
Xrefs

ICD10CM:H35.5

MESH:C563676

OMIM:610359

Synonyms

RP33 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal dominant disease

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