(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

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Identifiers

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2776512331
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MONDO:0008234
 
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