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Metadata
ID DOID:0110352
Name retinitis pigmentosa 59
Definition A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11.
https://www.ncbi.nlm.nih.gov/pubmed/21295283
Xrefs

ICD10CM:H35.5

MIM:613861

Synonyms

RP59 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

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