Peripheral retinal pigmentation abnormalities

Symptom Information:

Symptom ID: HPO:0200099
Synonyms:
Peripheral retinal pigmentation abnormalities [OMIM:Peripheral retinal pigmentation abnormalities]
Quality:
Cross references:
OMIM: "Peripheral retinal pigmentation abnormalities" [OMIM:Peripheral retinal pigmentation abnormalities]
Is a (Direct Parents):
HPO         Abnormality of retinal pigmentation
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)
                            Abnormality of retinal pigmentation(HPO:0007703)
                               Peripheral retinal pigmentation abnormalities(HPO:0200099)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Glutathione synthetase deficiency with 5-oxoprolinuria (Orphanet:289846)