Hyperaldosteronism, Familial, Type I (HALD1)

Hyperaldosteronism, Familial, Type I(来自ICD-11)

别称:

Glucocorticoid-Remediable Aldosteronism

Gra

Familial Hyperaldosteronism Type I

Glucocorticoid-Suppressible Hyperaldosteronism

Familial Hyperaldosteronism Type 1

Fh1

Acth-Dependent Hyperaldosteronism Syndrome

Aldosteronism, Glucocorticoid-Remediable

Glucocorticoid-Sensitive Hypertension

Glucocorticoid Sensitive Hypertension

Dexamethasone-Sensitive Hypertension

Dexamethasone Sensitive Hypertension

Hald1

Fh I

Fh-I

Gsh

Hyperaldosteronism, Glucocorticoid-Remediable

Aldosteronism, Sensitive to Dexamethasone

Aldosteronism Sensitive to Dexamethasone

Hyperaldosteronism, Familial Type 1

Hyperaldosteronism, Familial, 1

Familial Hyperaldosteronism 1

Familial Aldosteronism Type I

Fh Type 1

Grs

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hyperaldosteronism, Familial, Type I, also known as glucocorticoid-remediable aldosteronism, is related to familial hyperaldosteronism and hypertensive retinopathy. An important gene associated with Hyperaldosteronism, Familial, Type I is CYP11B1 (Cytochrome P450 Family 11 Subfamily B Member 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Cardiac conduction. The drug glucocorticoids has been mentioned in the context of this disorder. Affiliated tissues include kidney and heart, and related phenotypes are hypertension and dexamethasone-suppressible primary hyperaldosteronism

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