Hypertriglyceridemia 1 (HYTG1)

Alias:
Hypertriglyceridemia
Hypertriglyceridemia, Susceptibility to
Hypertriglyceridemia, Familial
Hytg1
Hypertriglyceridemias Familial
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypertriglyceridemia 1, also known as hypertriglyceridemia, is related to apolipoprotein c-ii deficiency and lipase deficiency, combined, and has symptoms including hypertriglyceridemic waist An important gene associated with Hypertriglyceridemia 1 is APOA5 (Apolipoprotein A5), and among its related pathways/superpathways are Metabolism and Olfactory Signaling Pathway. The drugs Metformin and Ciprofibrate have been mentioned in the context of this disorder. Affiliated tissues include heart and liver, and related phenotypes are hypertriglyceridemia and glucose intolerance
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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14
152
22

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
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