Preferred Label : Adrenal Gland Pheochromocytoma;
NCIt synonyms : Adrenal Gland Paraganglioma; Chromaffin Paraganglioma of the Adrenal Gland; Pheochromocytoma; Adrenal Pheochromocytoma; Adrenal Gland Chromaffin Paraganglioma; PCC; Intraadrenal Paraganglioma; Adrenal Gland Chromaffinoma; Adrenal Medullary Pheochromocytoma; Adrenal Medullary Paraganglioma;
NCIt related terms : Pheochromocytoma (adrenal);
NCIt definition : A neuroendocrine neoplasm of the sympathetic nervous system that arises from the chromaffin
cells of the adrenal medulla and secretes catecholamines. Clinical presentation includes
headaches, palpitations, chest and abdominal pain, hypertension, fever, and tremor.
Microscopically, a characteristic nesting (zellballen) growth pattern is usually seen.
Other growth patterns including trabecular pattern may also be present.;
Alternative definition : NCI-GLOSS: Tumor that forms in the center of the adrenal gland (gland located above
the kidney) that causes it to make too much adrenaline. Pheochromocytomas are usually
benign (not cancer) but can cause high blood pressure, pounding headaches, heart palpitations,
flushing of the face, nausea, and vomiting.;
Neoplastic status : Undetermined;
ICD-O code : 8700/0;
Codes from synonyms : 10034876; CDR0000322877;
Origin ID : C3326;
UMLS CUI : C4551683;
- Currated CISMeF NLP mapping
- Disease excludes abnormal cell
- Disease may have findings
- False automatic mappings
- HPO term
- Has associated anatomic sites
- Semantic type(s)
- UMLS correspondences (same concept)
- associated_with_malfunction_of_gene_product
- concept_is_in_subset
- 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
- may_be_associated_disease_of_disease