Visualize Submit Comment
Metadata
ID DOID:0110397
Name retinitis pigmentosa 27
Definition A retinitis pigmentosa that has_material_basis_in mutation in the NRL gene on chromosome 14q11.
https://www.ncbi.nlm.nih.gov/pubmed/10192380
Xrefs

ICD10CM:H35.5

MESH:C563526

OMIM:613750

Synonyms

RP27 [EXACT]

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal dominant disease

Add an item to the term tracker