Multiple Endocrine Neoplasia Type 2

Preferred Label : Multiple Endocrine Neoplasia Type 2;

NCIt definition : Multiple endocrine neoplasia caused by mutation of the RET gene. It includes the following neoplastic processes: multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, and hereditary thyroid gland medullary carcinoma.;

Neoplastic status : Undetermined;

Details

Origin ID

C123329;

UMLS CUI

C4048306;

Automatic exact mappings (from CISMeF team)
- multiple endocrine neoplasia type 2a [MeSH Descriptor]
Currated CISMeF NLP mapping
- Multiple endocrine neoplasia Type 2 [MedDRA Preferred Term]
- Multiple endocrine neoplasia type 2 [ORDO Disease]
- Multiple endocrine neoplasia type 2 [ICD-11 More detail]
- Multiple endocrine neoplasia, type 2 (disorder) [SNOMED CT concept]
- multiple endocrine neoplasia, type 2 [SNOMED Notion]
Disease excludes abnormal cell
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease excludes normal cell origin
- Thyroid Gland Follicular Cell [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- MEA Type II [MedDRA LLT]
- MEN Type II [MedDRA LLT]
- Multiple endocrine adenomatosis Type II [MedDRA LLT]
- Multiple endocrine neoplasia Type 2 [MedDRA Preferred Term]
- Multiple endocrine neoplasia Type II [MedDRA LLT]
- Multiple endocrine neoplasia, type 2 (disorder) [SNOMED CT concept]
- multiple endocrine neoplasia type 2 [Disease (Nov.)]
concept_is_in_subset
- CCPS Disease Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Endocrine Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_associated_disease
- Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
disease_has_finding
- Endocrine Differentiation [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Multifocal Lesion [NCIt concept]
disease_has_molecular_abnormality
- RET Gene Mutation [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_mapped_to_gene
- RET Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- RET Gene [NCIt concept]
- RET wt Allele [NCIt concept]
related_to_genetic_biomarker
- RET Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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