Hyperaldosteronism, Familial, Type Iii (HALD3)

Alias:
Familial Hyperaldosteronism Type Iii
Familial Hyperaldosteronism Type 3
Fh3
Fh Iii
Fh-Iii
Hald3
Hyperaldosteronism, Familial, 3
Familial Hyperaldosteronism 3
Fh Type Iii
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperaldosteronism, Familial, Type Iii, also known as familial hyperaldosteronism type iii, is related to familial hyperaldosteronism and hypercholesterolemia, familial, 3. An important gene associated with Hyperaldosteronism, Familial, Type Iii is KCNJ5 (Potassium Inwardly Rectifying Channel Subfamily J Member 5). Affiliated tissues include adrenal gland and kidney, and related phenotypes are hypertension and abnormal circulating renin
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Infant
<1/1000000
1
2
10

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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