Hyperlipidemia

Symptom Information:

Symptom ID: HPO:0003077
Synonyms:
Hyperlipidemia (disorder) [Orphanet:49480]
Hyperlipidaemia [HPO:0003077]
Hyperlipidemia [Orphanet:49480]
Hyperlipidemia [OMIM:Hyperlipidemia]
Hyperlipidemia/hypercholesterolemia/hypertriglyceridemia [Orphanet:49480]
Hyperlipidaemia [Orphanet:49480]
Hyperlipidaemia [MedDRA:10062060]
Hyperlipaemia [MedDRA:10062060]
Hyperlipemia [MedDRA:10062060]
Hyperlipidaemia NOS [MedDRA:10062060]
Hyperlipidaemia secondary [MedDRA:10062060]
Hyperlipidaemia, other and unspecified [MedDRA:10062060]
Hyperlipidemia [MedDRA:10062060]
Hyperlipoproteinemia [MedDRA:10062060]
Other and unspecified hyperlipidaemia [MedDRA:10062060]
Other and unspecified hyperlipidemia [MedDRA:10062060]
Hyperlipidemia secondary [MedDRA:10062060]
Hyperlipoproteinaemia [MedDRA:10062060]
Lipemia [MedDRA:10062060]
Lipaemia [MedDRA:10062060]
Hyperlipemia [OMIM:Hyperlipemia]
Quality:
Cross references:
Orphanet:49480 "Hyperlipidemia/hypercholesterolemia/hypertriglyceridemia" [Orphanet:49480]
OMIM: "Hyperlipidemia" [OMIM:Hyperlipidemia]
OMIM: "Hyperlipemia" [OMIM:Hyperlipemia]
UMLS:C0020473 "Hyperlipidaemia" [HPO:0003077]
UMLS:C0020473 "Hyperlipidemia" [Orphanet:49480]
Is a (Direct Parents):
HPO         Abnormality of lipid metabolism
Orphanet Abnormality of lipid metabolism
MedDRA Hyperlipidaemias NEC
HPO         Increased serum testosterone level
Orphanet Hypertriglyceridemia
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)