Conn's Syndrome

Alias:
Hyperaldosteronism
Cushing Syndrome
Primary Hyperaldosteronism
Primary Aldosteronism
Hypercortisolism
Cushing's Syndrome
Cushing Disease
Conn Syndrome
Pituitary Corticotroph Micro-Adenoma
Pituitary-Dependent Cushing Syndrome
Corticotroph Pituitary Adenoma
Pituitary Acth Hypersecretion
Hyperadrenocorticism
Ectopic Acth - [adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
Primary Aldosteronism Due to Bilateral Adrenal Hyperplasia
Ectopic Acth - [adrenocorticotropic Hormone] Secretion
Cushing Syndrome Secondary to Ectopic Acth-Secretion
Primary Aldosteronism Due to Adrenal Hyperplasia
Pituitary-Dependant Hypercortisolism Disorder
Hypercortisolism Due to Nonpituitary Tumour
Pituitary-Dependant Cushing Syndrome
Pituitary-Dependant Hypercortisolism
Corticoadrenal Hypersecretion
Adrenal Gland Hyperfunction
Pituitary Cushing Syndrome
Adrenal Cushing's Syndrome
Adrenal Cortical Adenoma
Ectopic Cushing Syndrome
Idiopathic Aldosteronism
Cortisol Hypersecretion
Acth Syndrome, Ectopic
Aldosteronism Primary
Cushing Syndrome Nos
Cushing's Disease
Aldosteronism
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Conn's Syndrome, also known as hyperaldosteronism, is related to ectopic cushing syndrome and pigmented nodular adrenocortical disease, primary, 1, and has symptoms including cushingoid facies An important gene associated with Conn's Syndrome is USP8 (Ubiquitin Specific Peptidase 8), and among its related pathways/superpathways are Infectious disease and Metabolism. The drugs Bromocriptine and Liraglutide have been mentioned in the context of this disorder. Affiliated tissues include pituitary and adrenal gland, and related phenotypes are increased circulating cortisol level and paradoxical increased cortisol secretion on dexamethasone suppression test
Related ID:
MESH:D003480
ICD11:1646144829

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
1-9/100000
125
1389
18

Medical Symptom

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

Gene & Mutation

#
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
No Data Found!
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