Lipemia retinalis

Symptom Information:

Symptom ID: HPO:0000660
Synonyms:
Lipemia retinalis [OMIM:Lipemia retinalis]
Lipemia retinalis (in severe cases) [OMIM:Lipemia retinalis (in severe cases)]
Quality:
Cross references:
OMIM: "Lipemia retinalis" [OMIM:Lipemia retinalis]
OMIM: "Lipemia retinalis (in severe cases)" [OMIM:Lipemia retinalis (in severe cases)]
Is a (Direct Parents):
HPO         Abnormality of the retina
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:
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)