(Q604075)
English
multiple endocrine neoplasia type 2A
autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis
- MEN2A
- multiple endocrine neoplasia II
- MEA Type II
- MEA Type 2a
- Pheochromocytoma and Amyloid-Producing Medullary Thyroid Carcinoma
- Pheochromocytoma and amyloid producing medullary thyroid carcinoma
- Multiple Endocrine Adenomatosis Type II
- Multiple Endocrine Neoplasia Type 2a
- Multiple Endocrine Adenomatosis Type 2a
- Ptc Syndrome
- Thyroid Carcinoma, Familial Medullary
- MEN-2A syndrome
- Multiple Endocrine Neoplasia, Type II
- Multiple Endocrine Neoplasia Type II
- MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
- MEN Type II
- MEN Type 2a
- Multiple Endocrine Adenomatosis, Type II
- MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A
- MEN 2A
- Sipple s Игорьyndrome
Statements
1 reference
1 reference
1 reference
28 July 2018
MONDO:0008234
1 reference
28 July 2018
MONDO:0008234
4 references
258.02
2 references
28 July 2018
MONDO:0008234
C3226
1 reference
1 reference
Identifiers
Multiple Endocrine Neoplasia Type 2a
1 reference
28 July 2018
MONDO:0008234
1 reference
1 reference
28 July 2018
MONDO:0008234
2 references
28 July 2018
MONDO:0008234
1 reference
28 July 2018
MONDO:0008234
2776512331
0 references
MONDO:0008234
1 reference
28 July 2018
MONDO:0008234
1 reference
1 reference
1 reference
1 reference
28 July 2018
MONDO:0008234
1 reference