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Metadata
ID DOID:0110368
Name retinitis pigmentosa 26
Definition A retinitis pigmentosa that has_material_basis_in mutation in the CERKL gene on chromosome 2q31.
https://www.ncbi.nlm.nih.gov/pubmed/14681825
Xrefs

ICD10CM:H35.5

MESH:C564249

OMIM:608380

Synonyms

RP26 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

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