Hypertriglyceridemia

Symptom Information:

Symptom ID: HPO:0002155
Synonyms:
Increased plasma triglycerides [HPO:0002155]
Increased serum triglycerides [HPO:0002155]
Increased triglycerides [HPO:0002155]
Hypertriglyceridemia (disorder) [Orphanet:49480]
Hypertriglyceridemia [Orphanet:49480]
Hypertriglyceridemia [OMIM:Hypertriglyceridemia]
Increased plasma triglycerides [OMIM:Increased plasma triglycerides]
Increased serum triglycerides [OMIM:Increased serum triglycerides]
Increased triglycerides [OMIM:Increased triglycerides]
Hyperlipidemia/hypercholesterolemia/hypertriglyceridemia [Orphanet:49480]
Hypertriglyceridaemia [Orphanet:49480]
Hypertriglyceridaemia [MedDRA:10020869]
Hypertriglyceridemia [MedDRA:10020869]
Pure hyperglyceridaemia [MedDRA:10020869]
Pure hyperglyceridemia [MedDRA:10020869]
Hyperglyceridaemia [MedDRA:10020869]
Hyperglyceridemia [MedDRA:10020869]
Increased serum triglycerides (in some patients) [OMIM:Increased serum triglycerides (in some patients)]
Increased triglycerides (less common) [OMIM:Increased triglycerides (less common)]
Quality:
Cross references:
Orphanet:49480 "Hyperlipidemia/hypercholesterolemia/hypertriglyceridemia" [Orphanet:49480]
OMIM: "Hypertriglyceridemia" [OMIM:Hypertriglyceridemia]
OMIM: "Increased plasma triglycerides" [OMIM:Increased plasma triglycerides]
OMIM: "Increased serum triglycerides" [OMIM:Increased serum triglycerides]
OMIM: "Increased triglycerides" [OMIM:Increased triglycerides]
OMIM: "Increased serum triglycerides (in some patients)" [OMIM:Increased serum triglycerides (in some patients)]
OMIM: "Increased triglycerides (less common)" [OMIM:Increased triglycerides (less common)]
UMLS:C0020557 "Hypertriglyceridemia" [Orphanet:49480]
Is a (Direct Parents):
HPO         Hyperlipidemia
Orphanet Abnormality of lipid metabolism
MedDRA Elevated triglycerides
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)
                Hypertriglyceridemia(HPO:0002155)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Abnormality of lipid metabolism(HPO:0003119)
       Elevated triglycerides(MedDRA:10014486)
          Hypertriglyceridemia(HPO:0002155)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Metabolic and nutritional disorders congenital(MedDRA:10027424)
       Abnormality of lipid metabolism(HPO:0003119)
          Elevated triglycerides(MedDRA:10014486)
             Hypertriglyceridemia(HPO:0002155)
Database Frequency: 67 / 7739
Resource:

All diseases associated with this symptom:

APOLIPOPROTEIN E (OMIM:107741)
ATHEROSCLEROSIS SUSCEPTIBILITY (OMIM:108725)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alström syndrome (Orphanet:64)
Ataxia with vitamin E deficiency (Orphanet:96)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 7 (OMIM:615984)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CANDLE syndrome (Orphanet:325004)
Citrullinemia type II (Orphanet:247585)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Cushing syndrome (Orphanet:553)
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY (OMIM:615924)
Erythropoietic protoporphyria (Orphanet:79278)
Familial LCAT deficiency (Orphanet:79293)
Familial apolipoprotein C-II deficiency (Orphanet:309020)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
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)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Fish-eye disease (Orphanet:79292)
GLYCOGEN STORAGE DISEASE IXc (OMIM:613027)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
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 liver phosphorylase kinase deficiency (Orphanet:264580)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3 (OMIM:608898)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 (OMIM:603552)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5 (OMIM:613101)
HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS (OMIM:144300)
HYPERTRIGLYCERIDEMIA, FAMILIAL (OMIM:145750)
Hemochromatosis type 3 (Orphanet:225123)
Hyperlipoproteinemia type 4 (Orphanet:413)
Infantile regressive hypertriglyceridemia and hepatosteatosis (Orphanet:300293)
Isolated glycerol kinase deficiency (Orphanet:408)
JMP syndrome (Orphanet:324999)
LCAT deficiency (Orphanet:650)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
MOVED TO 143890 (OMIM:144400)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Maternally-inherited diabetes and deafness (Orphanet:225)
Nakajo-Nishimura syndrome (Orphanet:2615)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Neutral lipid storage myopathy (Orphanet:98908)
Niemann-Pick disease type B (Orphanet:77293)
Niemann-Pick disease type E (Orphanet:99022)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
Proteasome disability syndrome (Orphanet:324977)
Smith-Magenis syndrome (Orphanet:819)
TEMPLE SYNDROME (OMIM:616222)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
X-linked lymphoproliferative disease (Orphanet:2442)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)