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Metadata
ID DOID:0110415
Name retinitis pigmentosa 2
Definition A retinitis pigmentosa that has_material_basis_in mutation in the RP2 gene on chromosome Xp11.3.
https://www.ncbi.nlm.nih.gov/pubmed/9697692
Xrefs

ICD10CM:H35.5

MESH:C567523

OMIM:312600

Synonyms

RP2 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a X-linked monogenic disease

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