Pigmentary retinal degeneration
Symptom Information:
Symptom ID: | HPO:0001146 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |