Hyperaldosteronism, Familial, Type Ii (HALD2)

Alias:
Familial Hyperaldosteronism Type Ii
Familial Hyperaldosteronism Type 2
Fh-Ii
Familial Adrenal Adenoma
Hald2
Fh Ii
Fh2
Hyperaldosteronism Familial Type 2
Hyperaldosteronism, Familial, 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperaldosteronism, Familial, Type Ii, also known as familial hyperaldosteronism type ii, is related to familial hyperaldosteronism and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Hyperaldosteronism, Familial, Type Ii is CLCN2 (Chloride Voltage-Gated Channel 2). Related phenotypes are hypertension and glucocortocoid-insensitive primary hyperaldosteronism
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
2
23
5

Medical Symptom

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

Gene & Mutation

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Mutations
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Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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