loading...| Preferred Name |
Familial medullary thyroid carcinoma |
|
| Synonyms |
Medullary thyroid cancer, familial Thyroid Carcinoma, Familial Medullary Thyroid cancer, familial medullary |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C536911 |
|
| altLabel |
Medullary thyroid cancer, familial Thyroid Carcinoma, Familial Medullary Thyroid cancer, familial medullary |
|
| cui |
C1833921 |
|
| Has mapping qualifier | ||
| HM |
D018813 D013964 D018276/Q000151 |
|
| Inverse of RB |
0 |
|
| Mapped to |
http://purl.bioontology.org/ontology/MESH/D018276 |
|
| MDA |
20100825 |
|
| MeSH Frequency |
113 |
|
| 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 |
T740843 T803046 T740842 T740841 |
|
| TH |
OMIM (2013) ORD (2010) |
|
| tui |
T191 |