Hypoalphalipoproteinemia, Primary, 2, Intermediate (FHA2I)

Alias:
Hypoalphalipoproteinemia, Primary, 2, Autosomal Dominant
Fha2i
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypoalphalipoproteinemia, Primary, 2, Intermediate, also known as hypoalphalipoproteinemia, primary, 2, autosomal dominant, is related to hypoalphalipoproteinemia, primary, 2 and hypoalphalipoproteinemia. An important gene associated with Hypoalphalipoproteinemia, Primary, 2, Intermediate is APOA1 (Apolipoprotein A1). Related phenotypes are decreased hdl cholesterol concentration and decreased circulating apolipoprotein a-i concentration
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
8
12

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

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PMID
Journal
Year
IF
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