Disease #03471 (RP59;CDG1BB (retinitis pigmentosa, type 59 (RP59, glycosylation, congenital disorder of, type Ibb (CDG1BB))), OMIM:613861)
Official abbreviation |
RP59;CDG1BB |
Name |
retinitis pigmentosa, type 59 (RP59, glycosylation, congenital disorder of, type Ibb (CDG1BB)) |
OMIM ID |
613861 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
DHDDS |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|