Lipemia retinalis
Symptom Information:
Symptom ID: | HPO:0000660 | ||
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) Lipemia retinalis(HPO:0000660) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Familial apolipoprotein C-II deficiency | (Orphanet:309020) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HYPERLIPOPROTEINEMIA, TYPE ID | (OMIM:615947) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |