Hereditary Adrenal Gland Pheochromocytoma

Preferred Label : Hereditary Adrenal Gland Pheochromocytoma;

NCIt synonyms : Familial Adrenal Gland Pheochromocytoma;

NCIt definition : A hereditary adrenal gland pheochromocytoma caused by mutations in SDHB, SDHC, and SDHD genes.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL936883;

Détails

Origin ID

C157248;

UMLS CUI

C4763508;

Disease excludes abnormal cell
- Large Osteoclastic Giant Cell [NCIt concept]
- Neoplastic Endothelial 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]
- Multifocal Lesion [NCIt concept]
- Nesting (Zellballen) Growth Pattern [NCIt concept]
- Palpitation [NCIt concept]
- Trabecular Pattern [NCIt concept]
- Tremor [NCIt concept]
Has associated anatomic sites
- Adrenal Gland [NCIt concept]
- Endocrine Gland [NCIt concept]
- Endocrine System [NCIt concept]
- Nervous System [NCIt concept]
- Peripheral Nervous System [NCIt concept]
- Peritoneum and Retroperitoneum [NCIt concept]
- Retroperitoneum [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_normal_tissue_origin
- Adrenal Cortex [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Chromaffin Cell [NCIt concept]
- Neoplastic Neuroendocrine Cell [NCIt concept]
disease_has_associated_disease
- Hereditary Paraganglioma-Pheochromocytoma Syndrome [NCIt concept]
disease_has_finding
- Epithelial Component Present [NCIt concept]
- Expression of Neuroendocrine Markers Present [NCIt concept]
- Hereditary Lesion [NCIt concept]
- Neuroendocrine Differentiation [NCIt concept]
disease_has_molecular_abnormality
- SDH Complex Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Chromaffin Cell [NCIt concept]
- Neural Crest-Derived Cell [NCIt concept]
disease_has_normal_tissue_origin
- Adrenal Medulla [NCIt concept]
disease_has_primary_anatomic_site
- Adrenal Gland [NCIt concept]
- Autonomic Nervous System [NCIt concept]
- Endocrine Gland [NCIt concept]
- Peripheral Nerve [NCIt concept]
- Sympathetic Nervous System [NCIt concept]
disease_mapped_to_gene
- SDHA Gene [NCIt concept]
- SDHAF2 Gene [NCIt concept]
- SDHB Gene [NCIt concept]
- SDHC Gene [NCIt concept]
- SDHD Gene [NCIt concept]
disease_may_have_molecular_abnormality
- SDHA Gene Mutation [NCIt concept]
- SDHAF2 Gene Mutation [NCIt concept]
- SDHB Gene Mutation [NCIt concept]
- SDHC Gene Mutation [NCIt concept]
- SDHD Gene Mutation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients