Adrenal Gland Pheochromocytoma

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;

Details

Origin ID

C3326;

UMLS CUI

C4551683;

Currated CISMeF NLP mapping
- Adrenal pheochromocytoma [HPO term]
- PHAEOCHROMOCYTOMA [WHO-ART Preferred Term]
- Phaeochromocytoma [ICD-11 More detail]
- Phaeochromocytoma [MedDRA Preferred Term]
- Pheochromocytoma [PASCAL descriptor]
- Pheochromocytoma [OMIM Phenotype]
- Pheochromocytoma [ICD-O code]
- Pheochromocytoma [HPO term]
- Pheochromocytoma [MedDRA LLT]
- Pheochromocytoma (disorder) [SNOMED CT concept]
- adrenal gland pheochromocytoma [DO Concept]
- pheochromocytoma [Disease (Nov.)]
- pheochromocytoma [DO Concept]
- pheochromocytoma [MedlinePlus Topic]
- pheochromocytoma [MeSH Descriptor]
- pheochromocytoma [MeSH concept]
- pheochromocytoma [Radlex concept]
- pheochromocytoma, nos [SNOMED Notion]
Disease excludes abnormal cell
- Large Osteoclastic Giant Cell [NCIt concept]
- Neoplastic Endothelial Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease excludes normal cell origin
- Endothelial Cell [NCIt concept]
Disease may have findings
- Abdominal Pain [NCIt concept]
- Chest Pain [NCIt concept]
- Fever [NCIt concept]
- Headache [NCIt concept]
- Hypertension [NCIt concept]
- Nesting (Zellballen) Growth Pattern [NCIt concept]
- Palpitation [NCIt concept]
- Trabecular Pattern [NCIt concept]
- Tremor [NCIt concept]
False automatic mappings
- 1-piperidinocyclohexanecarbonitrile (substance) [SNOMED CT concept]
- Pheochromocytoma (morphologic abnormality) [SNOMED CT concept]
HPO term
- Adrenal pheochromocytoma [HPO term]
- Pheochromocytoma [HPO term]
Has associated anatomic sites
- Adrenal Gland [NCIt concept]
- Nervous System [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Adrenal pheochromocytoma [HPO term]
- Chromaffin cell neoplasm (morphologic abnormality) [SNOMED CT concept]
- Phaeochromocytoma [MedDRA Preferred Term]
- Pheochromocytoma [MedDRA LLT]
- Pheochromocytoma (disorder) [SNOMED CT concept]
- Pheochromocytoma (morphologic abnormality) [SNOMED CT concept]
associated_with_malfunction_of_gene_product
- Proto-Oncogene Tyrosine-Protein Kinase Receptor Ret [NCIt concept]
- Secretogranin-1 [NCIt concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
- NCI CTEP SDC Neuroendocrine Cancer Sub-Category Terminology [NCIt concept]
- NCI CTEP Simplified Disease Classification Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_excludes_normal_tissue_origin
- Adrenal Cortex [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Chromaffin Cell [NCIt concept]
- Neoplastic Endocrine Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Neuroendocrine Cell [NCIt concept]
disease_has_associated_gene
- CHGB Gene [NCIt concept]
- CHGB wt Allele [NCIt concept]
- RET Gene [NCIt concept]
- RET wt Allele [NCIt concept]
disease_has_finding
- Endocrine Differentiation [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Expression of Neuroendocrine Markers Present [NCIt concept]
- Neuroendocrine Differentiation [NCIt concept]
disease_has_normal_cell_origin
- Chromaffin Cell [NCIt concept]
- Epithelial Cell [NCIt concept]
- Neural Crest-Derived Cell [NCIt concept]
disease_has_normal_tissue_origin
- Adrenal Medulla [NCIt concept]
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Adrenal Gland [NCIt concept]
- Autonomic Nervous System [NCIt concept]
- Peripheral Nerve [NCIt concept]
- Sympathetic Nervous System [NCIt concept]
may_be_associated_disease_of_disease
- Multiple Endocrine Neoplasia Type 2A [NCIt concept]
- Multiple Endocrine Neoplasia Type 2B [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]

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