multiple endocrine neoplasia type 2A
(Q604075)
autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis
autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis
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Current Data About
multiple endocrine neoplasia type 2A
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q18553439)
(Q1553018)
(Q55788491)
(Q55785849)
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| (P1692) |
258.02
|
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| (P1995) |
(Q162555)
|
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| (P2293) |
(Q18253720)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050430
http://identifiers.org/doid/DOID:0050430
http://www.orpha.net/ORDO/Orphanet_247698 http://www.orpha.net/ORDO/Orphanet_653 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
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 |
| description | autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis |
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