Tapetoretinal degeneration

Symptom Information:

Symptom ID: HPO:0000547
Synonyms:
Tapetoretinal degeneration [OMIM:Tapetoretinal degeneration]
Quality:
Cross references:
OMIM: "Tapetoretinal degeneration" [OMIM:Tapetoretinal degeneration]
Is a (Direct Parents):
HPO         Retinal degeneration
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:
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)