Tapetoretinal degeneration
Symptom Information:
Symptom ID: | HPO:0000547 | ||
Synonyms: |
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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) Retinal degeneration(HPO:0000546) Tapetoretinal degeneration(HPO:0000547) MedDRA: |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Ataxia - tapetoretinal degeneration | (Orphanet:1178) |
Dubowitz syndrome | (Orphanet:235) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
HOOFT DISEASE | (OMIM:236300) |
Joubert syndrome 5 | (OMIM:610188) |
Monosomy 18q | (Orphanet:1600) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Senior-Loken syndrome | (Orphanet:3156) |
Senior-Loken syndrome 1 | (OMIM:266900) |
Senior-Loken syndrome 3 | (OMIM:606995) |
Senior-Loken syndrome 6 | (OMIM:610189) |