A retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21. [ http://www.ncbi.nlm.nih.gov/pubmed/1749427 DOID:0110383 ]

This is just here as a test because I lose it

Term information

database cross reference
Subsets

gard_rare

abbreviation
RP7 [ MONDO:Lexical DOID:0110383 https://omim.org/entry/608133 ]

closeMatch

http://linkedlifedata.com/resource/umls/id/C2675552

http://linkedlifedata.com/resource/umls/id/C2675553

definition

A retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21.

exactMatch

http://purl.obolibrary.org/obo/DOID_0110383

http://identifiers.org/omim/608133

http://linkedlifedata.com/resource/umls/id/C1842475

has exact synonym

retinitis pigmentosa 7

retinitis pigmentosa type 7

RP7

has related synonym

Leber congenital amaurosis 18

RP 7

retinitis pigmentosa 7, digenic

id

MONDO:0011974

seeAlso

https://rarediseases.info.nih.gov/diseases/10386/retinitis-pigmentosa-7