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Metadata
ID DOID:0110358
Name retinitis pigmentosa 12
Definition A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3.
https://www.ncbi.nlm.nih.gov/pubmed/10508521
Xrefs

ICD10CM:H35.5

MESH:C563999

MIM:600105

Synonyms

RP12 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

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