Precocious atherosclerosis

Symptom Information:

Symptom ID: HPO:0004416
Synonyms:
Premature atherosclerosis [HPO:0004416]
Precocious atherosclerosis [OMIM:Precocious atherosclerosis]
Arterial atheroma/precocious atherosclerosis/arteriosclerosis [Orphanet:35510]
Quality:
Cross references:
HPO:0005177 "Premature arteriosclerosis" [Orphanet:35510]
Orphanet:35510 "Arterial atheroma/precocious atherosclerosis/arteriosclerosis" [Orphanet:35510]
OMIM: "Precocious atherosclerosis" [OMIM:Precocious atherosclerosis]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
Orphanet Atherosclerosis
HPO         Atherosclerosis
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:
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)