Hypertriglyceridemia
Symptom Information:
Symptom ID: | HPO:0002155 | |||||||||||||||||||
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) 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) |