Central tapetoretinal dystrophy

Symptom Information:

Symptom ID: HPO:0007982
Synonyms:
Central tapetoretinal dystrophy [OMIM:Central tapetoretinal dystrophy]
Quality:
Cross references:
OMIM: "Central tapetoretinal dystrophy" [OMIM:Central tapetoretinal dystrophy]
Is a (Direct Parents):
HPO         Retinal dystrophy
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 dystrophy(HPO:0000556)
                            Central tapetoretinal dystrophy(HPO:0007982)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Ruvalcaba syndrome (Orphanet:3121)