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GENATLAS PHENOTYPE
last update : 19/07/2006
Symbol MEN2A
Location 10q11.21
Name endocrine neoplasia, multiple, type IIA
Other name(s)
  • Sipple disease
  • pheochromocytoma and amyloid-producing medullary thyroid carcinoma
  • Corresponding gene RET
    Other symbol(s) MEN2
    Genetic determination autosomal dominant
    Function/system disorder endocrinology
    Type malignancy
    Gene product
    Name receptor tyrosine kinase with cadherin homology domain (RET)
    Remark(s)