Acth-Independent Macronodular Adrenal Hyperplasia
Disease ID: disease_node_14167
Connections displayed (default: 10).
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| Dbxref | GARD:10824, ORDO:189427, SNOMEDCT_US_2023_03_01:720459002, UMLS_CUI:C2062388 |
|---|---|
| Subclassof | DOID_446 |
| Data Source | DOID |
| Synonyms | ACTH-independent macronodular adrenocortical hyperplasia, AIMAH, Cushing syndrome due to macronodular adrenal hyperplasia, MMAD, adrenocorticotropic hormone-independent macronodular adrenal hyperplasia, corticotropin-independent macronodular adrenal hyperplasia, massive macronodular adrenocortical disease, primary macronodular adrenal hyperplasia |
| Doid Label | ACTH-independent macronodular adrenal hyperplasia |
| Doid Description | A primary hyperaldosteronism characterized by multiple bilateral adrenocortical nodules that cause a striking enlargement of the adrenal gland and production of an excess of cortisol. |
| Disease Node Id | disease_node_14167 |
| Doid Id | DOID_0111622 |
| Label | Acth-Independent Macronodular Adrenal Hyperplasia |
- Incoming r'ship
SUBCLASS_OFto/from Acth-Independent Macronodular Adrenal Hyperplasia 2(ID:disease_node_14168) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Acth-Independent Macronodular Adrenal Hyperplasia 1(ID:disease_node_14169) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cushing Syndrome(ID:disease_node_2343) (Disease)