Abnormality of lipid metabolism

Symptom Information:

Symptom ID: HPO:0003119
Synonyms:
Dyslipidemia [HPO:0003119]
Lipid metabolism disorder [Orphanet:49460]
Inborn error of lipid metabolism [Orphanet:49500]
Disorder of lipid metabolism (disorder) [Orphanet:49460]
Dyslipidemia (disorder) [Orphanet:49460]
Dyslipidemias [Orphanet:49460]
Lipid Metabolism Disorders [Orphanet:49460]
Lipid Metabolism, Inborn Errors [Orphanet:49500]
Dyslipidemia [OMIM:Dyslipidemia]
Lipid metabolism anomalies [Orphanet:49460]
Lipidosis/sulfatidosis [Orphanet:49500]
Inborn errors of lipid metabolism [Orphanet:49500]
Lipid metabolism disorder [MedDRA:10061227]
Disorders of lipoid metabolism [MedDRA:10061227]
Fat disorder [MedDRA:10061227]
Lipid metabolism disorder NOS [MedDRA:10061227]
Other disorders of lipoid metabolism [MedDRA:10061227]
Unspecified disorder of lipoid metabolism [MedDRA:10061227]
Unspecified disorders of lipoid metabolism [MedDRA:10061227]
Lipidosis acquired [MedDRA:10061227]
Inborn errors of lipid metabolism [MedDRA:10059674]
Sulfatidosis [Orphanet:49500]
Lipid metabolism disorders [MedDRA:10013317]
Inborn error of lipid metabolism [MedDRA:10072272]
Quality:
Cross references:
Orphanet:49460 "Lipid metabolism anomalies" [Orphanet:49460]
Orphanet:49500 "Lipidosis/sulfatidosis" [Orphanet:49500]
OMIM: "Dyslipidemia" [OMIM:Dyslipidemia]
UMLS:C0242339 "Dyslipidemias" [Orphanet:49460]
UMLS:C0154251 "Lipid Metabolism Disorders" [Orphanet:49460]
UMLS:C0023772 "Lipid Metabolism, Inborn Errors" [Orphanet:49500]
UMLS:C1706192 "Sulfatidosis" [Orphanet:49500]
Is a (Direct Parents):
MedDRA Metabolic and nutritional disorders congenital
Orphanet Abnormality of metabolism/homeostasis
MedDRA Lipid metabolism and deposit disorders NEC
HPO         Abnormal level of phospholipids
HPO         Abnormality of metabolism/homeostasis
MedDRA Metabolism and nutrition disorders
HPO         Hypolipidemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of lipid metabolism(HPO:0003119)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Abnormality of lipid metabolism(HPO:0003119)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Metabolic and nutritional disorders congenital(MedDRA:10027424)
       Abnormality of lipid metabolism(HPO:0003119)
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
Acute intermittent porphyria (Orphanet:79276)
Adult Still's disease (Orphanet:829)
Alström syndrome (Orphanet:64)
Apolipoprotein A-I deficiency (Orphanet:425)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bietti crystalline dystrophy (Orphanet:41751)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Cerebrotendinous xanthomatosis (Orphanet:909)
Cholestasis - lymphedema (Orphanet:1414)
Cushing syndrome (Orphanet:553)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
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)
GM1 gangliosidosis (Orphanet:354)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Glycogen storage disease due to phosphorylase kinase deficiency (Orphanet:370)
Griscelli disease (Orphanet:381)
Griscelli disease type 1 (Orphanet:79476)
Griscelli disease type 2 (Orphanet:79477)
Growth hormone insensitivity syndrome (Orphanet:181393)
Hypoalphalipoproteinemia (Orphanet:31153)
Kennedy disease (Orphanet:481)
LCAT deficiency (Orphanet:650)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 (OMIM:615980)
Laron syndrome (Orphanet:633)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
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)
Maturity-onset diabetes of the young, type 2 (OMIM:125851)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Metachromatic leukodystrophy (Orphanet:512)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 4 (Orphanet:578)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Neutral lipid storage disease (Orphanet:165)
Oculocerebrorenal syndrome (Orphanet:534)
Partial acquired lipodystrophy (Orphanet:79087)
Primary lipodystrophy (Orphanet:90970)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Sialidosis type 1 (Orphanet:812)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Stiff skin syndrome (Orphanet:2833)
Subaortic stenosis - short stature (Orphanet:3191)
Tay-Sachs disease (Orphanet:845)
Uhl anomaly (Orphanet:3403)
Williams syndrome (Orphanet:904)