Disease #02387 (RP-19 (retinitis pigmentosa, type 19 (RP-19)), OMIM:601718)

Official abbreviation RP-19
Name retinitis pigmentosa, type 19 (RP-19)
OMIM ID 601718
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCA4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A