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Metadata
ID DOID:0110367
Name retinitis pigmentosa 38
Definition A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13.
https://www.ncbi.nlm.nih.gov/pubmed/11062461
Xrefs

ICD10CM:H35.5

OMIM:613862

Synonyms

RP38 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

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