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Metadata
ID DOID:0110399
Name retinitis pigmentosa 37
Definition A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.
https://www.ncbi.nlm.nih.gov/pubmed/17564971
Xrefs

ICD10CM:H35.5

MESH:C567005

OMIM:611131

Synonyms

RP37 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

is_a autosomal dominant disease

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