loading...| Preferred Name |
Familial medullary thyroid carcinoma |
| Synonyms |
Thyroid cancer, familial medullary |
| ID |
http://purl.bioontology.org/ontology/MESH/C536911 |
| altLabel |
Thyroid cancer, familial medullary Medullary thyroid cancer, familial Thyroid Carcinoma, Familial Medullary |
| cui |
C1833921 |
| Has mapping qualifier | |
| HM |
D013964 D018276/Q000151 D018813 |
| Inverse of RB |
0 |
| Mapped to |
http://purl.bioontology.org/ontology/MESH/D018276 |
| MDA |
20100825 |
| MeSH Frequency |
83 |
| MMR |
20150818 |
| notation |
C536911 |
| prefLabel |
Familial medullary thyroid carcinoma |
| SC |
3 |
| Scope Statement |
A malignant tumor of the CALCITONIN - secreting parafollicular C cells of the THYROID that occurs sporadically or as a component of the MULTIPLE ENDOCRINE NEOPLASIA (MEN) type 2 (OMIM: 171400)/familial medullary thyroid carcinoma (FMTC) syndromes. Germline mutations in the RET and NTRK1 genes have been identified. OMIM: 155240 |
| TERMUI |
T740841 T803046 T740843 T740842 |
| TH |
ORD (2010) OMIM (2013) |
| tui |
T191 |