RS79853121 RET
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What This Variant Does
"Mutations of the RET-GDNF signaling pathway in Ondine's curse. [OMIM:?]
Associated Conditions
Hirschsprung disease
susceptibility to
1
Aganglionic megacolon
Multiple endocrine neoplasia type 2A
Multiple endocrine neoplasia type 2B
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia
type 2
Pheochromocytoma
Familial medullary thyroid carcinoma
Hirschsprung disease
susceptibility to
1
Aganglionic megacolon
Other Variants in RET