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Metadata
ID DOID:0110383
Name retinitis pigmentosa 7
Definition A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.
https://www.ncbi.nlm.nih.gov/pubmed/1749427
Xrefs

ICD10CM:H35.5

MESH:C564284

MIM:608133

Synonyms

RP7 [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a retinitis pigmentosa

is_a digenic disease

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some digenic inheritance

has material basis in some autosomal dominant inheritance

has material basis in some autosomal recessive inheritance

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