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Ontology Browser

Term:
multiple endocrine neoplasia type 2 (EFO:MONDO:0019003)
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Parent Terms Term With Siblings Child Terms
differentiated thyroid carcinoma +   
familial nonmedullary thyroid carcinoma +  
hereditary thyroid gland medullary carcinoma 
multiple endocrine neoplasia type 1 
multiple endocrine neoplasia type 2 +  
Multiple endocrine neoplasia type 2 (MEN2) is a multiple endocrine neoplasia, a polyglandular cancer syndrome characterized by the occurrence of medullary thyroid carcinoma (MTC), pheochromocytoma (PCC), in one variant, primary hyperparathyroidism (PHPT). There are three forms: MEN2A, MEN2B, and familial medullary thyroid carcinoma (FMTC).
multiple endocrine neoplasia type 4 
thyroid gland adenocarcinoma +   
Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation 
Thyroid Gland Squamous Cell Carcinoma 
Thyroid Gland Undifferentiated (Anaplastic) Carcinoma 

Synonyms
Exact Synonyms: MEN2 ;   NCIT:C123329 ;   Orphanet:653 ;   http://identifiers.org/medgen/887211 ;   http://identifiers.org/snomedct/61808009 ;   http://linkedlifedata.com/resource/umls/id/C4048306 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1837913809
Synonyms: http://identifiers.org/meddra/10028191
Alternate IDs: MONDO:0019003
Xrefs: GARD:3830 ;   ICD9:194.8 ;   ICD9:258.02 ;   MEDGEN:887211 ;   MedDRA:10028191 ;   NANDO:2200406 ;   NCI:C123329 ;   NORD:1467 ;   ORDO:653 ;   SCTID:61808009
see_also: https://rarediseases.info.nih.gov/diseases/3830/multiple-endocrine-neoplasia-type-2" xsd:anyURI {source="GARD:0003830
Definition Sources: Orphanet:653

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