Familial Apolipoprotein C-Ii Deficiency

Alias:
Familial Apoc-Ii Deficiency
Familial Apoc2 Deficiency
Hyperlipoproteinemia, Type Ib
Hyperlipoproteinemia, Type 1b
Hyperlipoproteinemia Type I
C-Ii Anapolipoproteinemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Apolipoprotein C-Ii Deficiency, also known as familial apoc-ii deficiency, is related to apolipoprotein c-ii deficiency and familial lipoprotein lipase deficiency. An important gene associated with Familial Apolipoprotein C-Ii Deficiency is APOC2 (Apolipoprotein C2), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Metabolism of water-soluble vitamins and cofactors. The drugs Neuroprotective Agents and Gastrointestinal Agents have been mentioned in the context of this disorder.
Related ID:
MESH:D008072

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Child
<1/1000000
11
62
14

Medical Symptom

#
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
No Data Found!
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