Hyperlipidemia, Familial Combined, 1 (FCHL1)

Alias:
Hyperlipidemia, Familial Combined, Susceptibility to
Hyperlipidemia, Familial Combined
Hyperlipidemia, Combined, 1
Hyplip1
Fchl1
Familial Combined Hyperlipidemia Type 1
Hyperlipoproteinemia Type Iib
Hyperlipidemia Combined, 1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperlipidemia, Familial Combined, 1, also known as hyperlipidemia, familial combined, susceptibility to, is related to hyperlipidemia, familial combined, 3 and lipid metabolism disorder. An important gene associated with Hyperlipidemia, Familial Combined, 1 is USF1 (Upstream Transcription Factor 1), and among its related pathways/superpathways is Familial hyperlipidemia type 1. The drugs Fenofibrate and Lovastatin have been mentioned in the context of this disorder. Affiliated tissues include heart.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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2
18
21

Medical Symptom

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

Gene & Mutation

#
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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