Precocious atherosclerosis
Symptom Information:
Symptom ID: | HPO:0004416 | ||||||
Synonyms: |
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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 cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Arteriosclerosis(HPO:0002634) Atherosclerosis(HPO:0002621) Precocious atherosclerosis(HPO:0004416) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
CADASIL | (Orphanet:136) |
Familial LCAT deficiency | (Orphanet:79293) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fish-eye disease | (Orphanet:79292) |
HYPERLIPOPROTEINEMIA, TYPE IV | (OMIM:144600) |
HYPERTRIGLYCERIDEMIA, FAMILIAL | (OMIM:145750) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hyperlipoproteinemia type 4 | (Orphanet:413) |
LCAT deficiency | (Orphanet:650) |
Werner syndrome | (Orphanet:902) |