Hyperlipidemia
Symptom Information:
Symptom ID: | HPO:0003077 | |||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||
Quality: | ||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of lipid metabolism(HPO:0003119) Hyperlipidemia(HPO:0003077) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Abnormality of lipid metabolism(HPO:0003119) Hyperlipidaemias NEC(MedDRA:10020666) Hyperlipidemia(HPO:0003077) Congenital, familial and genetic disorders(MedDRA:10010331) Metabolic and nutritional disorders congenital(MedDRA:10027424) Abnormality of lipid metabolism(HPO:0003119) Hyperlipidaemias NEC(MedDRA:10020666) Hyperlipidemia(HPO:0003077) |
|||||||||||||||||||||
Database Frequency: | 37 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ANALBUMINEMIA | (OMIM:616000) |
Alström syndrome | (Orphanet:64) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Cholestasis - lymphedema | (Orphanet:1414) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis | (Orphanet:94062) |
Cushing syndrome | (Orphanet:553) |
DIARRHEA 7 | (OMIM:615863) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 | (OMIM:603278) |
Familial LCAT deficiency | (Orphanet:79293) |
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes | (Orphanet:93216) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fish-eye disease | (Orphanet:79292) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
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) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Glycogen storage disease due to hepatic glycogen synthase deficiency | (Orphanet:2089) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
LCAT deficiency | (Orphanet:650) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
NEPHROTIC SYNDROME, TYPE 2 | (OMIM:600995) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |