Peripheral retinal pigmentation abnormalities
Symptom Information:
Symptom ID: | HPO:0200099 | ||
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) Abnormality of retinal pigmentation(HPO:0007703) Peripheral retinal pigmentation abnormalities(HPO:0200099) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Glutathione synthetase deficiency with 5-oxoprolinuria | (Orphanet:289846) |