Pigmentary retinal degeneration

Symptom Information:

Symptom ID: HPO:0001146
Synonyms:
Retinal pigmentary degeneration [HPO:0001146]
Pigmentary retinal degeneration [OMIM:Pigmentary retinal degeneration]
Retinal pigmentary degeneration [OMIM:Retinal pigmentary degeneration]
Quality:
Cross references:
OMIM: "Pigmentary retinal degeneration" [OMIM:Pigmentary retinal degeneration]
OMIM: "Retinal pigmentary degeneration" [OMIM:Retinal pigmentary degeneration]
Is a (Direct Parents):
HPO         obsolete Abnormality of the retinal pigment epithelium
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         obsolete Abnormality of the retinal pigment epithelium(HPO:0008051)
                            Pigmentary retinal degeneration(HPO:0001146)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Abetalipoproteinemia (Orphanet:14)
EXUDATIVE VITREORETINOPATHY 4 (OMIM:601813)
EXUDATIVE VITREORETINOPATHY 5 (OMIM:613310)
Familial exudative vitreoretinopathy (Orphanet:891)
Goldmann-Favre syndrome (Orphanet:53540)
Leber congenital amaurosis 10 (OMIM:611755)
MELAS (Orphanet:550)
Maternally-inherited diabetes and deafness (Orphanet:225)
RETINITIS PIGMENTOSA 47 (OMIM:613758)
RETINITIS PIGMENTOSA 7 (OMIM:608133)
RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT (OMIM:180210)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
Retinal degeneration - nanophthalmos - glaucoma (Orphanet:1574)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)