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RET/ELKS FUSION GENE CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 PHEOCHROMOCYTOMA, SOMATIC THYROID CARCINOMA, FAMILIAL MEDULLARY CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, WITH HIRSCHSPRUNG DISEASE RECLASSIFIED - VARIANT OF UNKNOWN SIGNIFICANCE MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA RET THYROID CARCINOMA, SPORADIC MEDULLARY RET PROTOONCOGENE HIRSCHSPRUNG DISEASE, PROTECTION AGAINST PHEOCHROMOCYTOMA
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