Preferred Label : Adrenal Cortical Carcinoma;
NCIt synonyms : Carcinoma of the Adrenal Cortex; Carcinoma of Adrenal Cortex;
NCIt related terms : CARCINOMA, ADRENOCORTICAL, MALIGNANT; Adrenal Cortex Adenocarcinoma; Adenocarcinoma, Adrenocortical, Malignant; adrenocortical cancer; cancer of the adrenal cortex; Adrenocortical carcinoma, NOS; Adrenal cortical adenocarcinoma; Adrenal Cortex Cancer; adrenocortical carcinoma; Cortical Cell Carcinoma; Adrenal Cortex Carcinoma;
NCIt definition : 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.;
Alternative definition : CDISC: A malignant epithelial neoplasm arising from adrenal cortical cells.; NCI-GLOSS: 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).;
Neoplastic status : Malignant;
ICD-O code : 8370/3;
Codes from synonyms : 10001327; CDR0000446526; CDR0000457974; CDR0000457975;
Origin ID : C9325;
UMLS CUI : C0206686;
- Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- DO Cross reference
- Disease excludes abnormal cell
- Disease may have findings
- Has associated anatomic sites
- Semantic type(s)
- UMLS correspondences (same concept)
- Validated automatic mappings to BTNT
- Validated automatic mappings to NTBT
- associated_with_malfunction_of_gene_product
- concept_is_in_subset
- disease_excludes_finding
- disease_excludes_normal_tissue_origin
- disease_has_abnormal_cell
- disease_has_associated_gene
- disease_has_finding
- disease_has_normal_cell_origin
- disease_has_normal_tissue_origin
- disease_has_primary_anatomic_site
- disease_mapped_to_gene
- disease_may_have_associated_disease
- disease_may_have_molecular_abnormality
- may_be_associated_disease_of_disease
- neoplasm_has_special_category
- pathogenesis_of_disease_involves_gene