Apolipoprotein C-Ii Deficiency (HLPP1B)

Alias:
Familial Apolipoprotein C-Ii Deficiency
Hyperlipoproteinemia, Type Ib
Apolipoprotein C-Ii
Apoc2 Deficiency
Hyperlipoproteinemia Type Ib
Apolipoprotein C2 Deficiency
Apolipoprotein C-Ii Variant
C-Ii Anapolipoproteinemia
Hyperlipoproteinemia 1b
Hlpp1b
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Apolipoprotein C-Ii Deficiency, also known as familial apolipoprotein c-ii deficiency, is related to familial apolipoprotein c-ii deficiency and hyperlipoproteinemia, type i. An important gene associated with Apolipoprotein C-Ii Deficiency is APOC2 (Apolipoprotein C2), and among its related pathways/superpathways are Metabolism of water-soluble vitamins and cofactors and Visual phototransduction. Affiliated tissues include smooth muscle and heart, and related phenotypes are splenomegaly and hypertriglyceridemia

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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2
9
26

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
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Gene & Mutation

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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