Acth-Independent Macronodular Adrenal Hyperplasia (AIMAH1)

Alias:
Cushing Syndrome Due to Macronodular Adrenal Hyperplasia
Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia
Corticotropin-Independent Macronodular Adrenal Hyperplasia
Acth-Independent Macronodular Adrenocortical Hyperplasia
Acth-Independent Macronodular Adrenal Hyperplasia 1
Aimah1
Hyperplasia, Adrenal, Acth-Independent, Macronodular, Type 1
Acth-Independent Macronodular Adrenal Hyperplasia 2
Primary Bilateral Macronodular Adrenal Hyperplasia
Massive Macronodular Adrenocortical Disease
Primary Macronodular Adrenal Hyperplasia
Cushing Syndrome, Adrenal, Due to Aimah
Adrenal Cushing Syndrome Due to Aimah
Acth-Independent Cushing Syndrome
Aimah
Mmad
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Acth-Independent Macronodular Adrenal Hyperplasia, also known as cushing syndrome due to macronodular adrenal hyperplasia, is related to acth-independent macronodular adrenal hyperplasia 1 and cushing syndrome due to bilateral macronodular adrenocortical disease, and has symptoms including agitation and generalized fatigue. An important gene associated with Acth-Independent Macronodular Adrenal Hyperplasia is GNAS (GNAS Complex Locus), and among its related pathways/superpathways are Class A/1 (Rhodopsin-like receptors) and GPCR downstream signalling. The drugs Racepinephrine and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include adrenal gland and pituitary, and related phenotypes are emotional lability and depression
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
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15
137
27

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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