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Results for Proteins associated with the Gene: RET
RET
5979


Known Diseases associated with this Protein:
  CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL
  CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, WITH HIRSCHSPRUNG DISEASE
  CONGENITAL CENTRAL HYPOVENTILATION SYNDROME (CCHS)
  HIRSCHSPRUNG DISEASE 1 (HSCR1)
  HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
  MEDULLARY THYROID CARCINOMA (MTC)
  MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
  MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE
  MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB
  MULTIPLE NEOPLASIA 2A (MEN2A)
  MULTIPLE NEOPLASIA 2B (MEN2B)
  PHEOCHROMOCYTOMA (PCC)
  PHEOCHROMOCYTOMA, INCLUDED
  PHEOCHROMOCYTOMA, SOMATIC, IN
  RENAL ADYSPLASIA (RADYS)
  RENAL AGENESIS
  THYROID CARCINOMA, FAMILIAL MEDULLARY
  THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
  THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED;;
  THYROID CARCINOMA, SPORADIC MEDULLARY, INCLUDED;;
157
17
44
1
129
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