Sipple syndrome

Sip·ple syn·drome

(sip'ĕl), [MIM*171400] pheochromocytoma, medullary carcinoma of the thyroid, and parathyroid adenomas; autosomal dominant inheritance, caused by mutation in the RET oncogene on chromosome 10q.

Sip·ple syn·drome

(sip'ĕl), [MIM*171400] pheochromocytoma, medullary carcinoma of the thyroid, and parathyroid adenomas; autosomal dominant inheritance, caused by mutation in the RET oncogene on chromosome 10q.

Sip·ple syn·drome

(sip'ĕl sin'drōm) Pheochromocytoma, medullary carcinoma of the thyroid, and parathyroid adenomas; autosomal dominant inheritance, caused by mutation in the RET oncogene on chromosome 10q.

Sipple,

John H., U.S. physician, 1930–. Sipple syndrome - pheochromocytoma, medullary carcinoma of the thyroid, and neural tumors. Synonym(s): multiple endocrine neoplasia, type 2

Sip·ple syn·drome

(sip'ĕl sin'drōm) [MIM*171400] Pheochromocytoma, medullary carcinoma of the thyroid, and parathyroid adenomas.