Hypoalphalipoproteinemia
Symptom Information:
Symptom ID: | HPO:0003233 | |||||||
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 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: |
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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) |