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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Adrenocortical Carcinoma

adrenocortical carcinoma

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Entity Type
Diseases
Relation Groups
4
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Basic Information

Grouped by core information, identifiers, and descriptions.

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Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Adrenocortical Carcinoma
Standard Disease Name
adrenocortical carcinoma
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D018268
OMIM ID
MTHU017416|MTHU016123
UMLS ID
C0206686
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A rare cancer that forms in the outer layer of tissue of the adrenal gland (a small organ on top of each kidney that makes steroid hormones, adrenaline, and noradrenaline to control heart rate, blood pressure, and other body functions).|NCI2016_CDISC_1602D:A malignant epithelial neoplasm arising from adrenal cortical cells.|NCI2016_02D:A rare, usually large (greater than 5cm), malignant epithelial tumor arising from the adrenal cortical cells. Symptoms are usually related to the excessive production of hormones, and include Cushing's syndrome and virilism in women. Common sites of metastasis include liver, lung, bone, and retroperitoneal lymph nodes. Advanced radiologic procedures have enabled the detection of small tumors, resulting in the improvement of the 5-year survival.|MSH2017_2016_08_12:A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM.|HPO2016_07_04:A malignant neoplasm of the adrenal cortex that may produce hormones such as cortisol, aldosterone, estrogen, or testosterone. [HPO:probinson]