Disease #03471

Official abbreviation RP-59;CDG-1BB
Name retinitis pigmentosa, type 59 (RP-59, glycosylation, congenital disorder of, type Ibb (CDG-1BB))
OMIM ID 613861
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DHDDS
Associated tissues -
Disease features autosomal recessive
Remarks -