Hypoalphalipoproteinemia

Symptom Information:

Symptom ID: HPO:0003233
Synonyms:
Decreased circulating high-density lipoprotein cholesterol [HPO:0003233]
Decreased HDL cholesterol [HPO:0003233]
Low HDL-cholesterol [HPO:0003233]
Decreased HDL cholesterol [OMIM:Decreased HDL cholesterol]
Hypoalphalipoproteinemia [OMIM:Hypoalphalipoproteinemia]
Low HDL-cholesterol [OMIM:Low HDL-cholesterol]
Low plasma HDL [OMIM,du]
Quality:
Cross references:
OMIM: "Decreased HDL cholesterol" [OMIM:Decreased HDL cholesterol]
OMIM: "Hypoalphalipoproteinemia" [OMIM:Hypoalphalipoproteinemia]
OMIM: "Low HDL-cholesterol" [OMIM:Low HDL-cholesterol]
Is a (Direct Parents):
HPO         Hypolipoproteinemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of lipid metabolism(HPO:0003119)
             Abnormality of cholesterol metabolism(HPO:0003107)
                Abnormality of the level of lipoprotein cholesterol(HPO:0010979)
                   Hypolipoproteinemia(HPO:0010981)
                      Hypoalphalipoproteinemia(HPO:0003233)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

ATHEROSCLEROSIS SUSCEPTIBILITY (OMIM:108725)
Alström syndrome (Orphanet:64)
Apolipoprotein A-I deficiency (Orphanet:425)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Familial LCAT deficiency (Orphanet:79293)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Fish-eye disease (Orphanet:79292)
Hyperlipoproteinemia type 5 (Orphanet:70470)
LCAT deficiency (Orphanet:650)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Maturity-onset diabetes of the young, type 1 (OMIM:125850)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Niemann-Pick disease type B (Orphanet:77293)
Niemann-Pick disease type E (Orphanet:99022)
Tangier disease (Orphanet:31150)