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Disease name, Applicable field
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Dermatology, cancer
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OMIM |
OMIM ID:
164761
Human Gene Symbol:
RET
Allelic Variant Name :
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB |
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HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 |
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA |
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA |
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CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, WITH HIRSCHSPRUNG DISEASE |
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THYROID CARCINOMA, FAMILIAL MEDULLARY |
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CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL |
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE |
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HIRSCHSPRUNG DISEASE, PROTECTION AGAINST |
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RENAL AGENESIS |
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH CUTANEOUS LICHEN AMYLOIDOSIS |
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