multiple endocrine neoplasia type 2B
(Q624748)
autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities
autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities
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Current Data About
multiple endocrine neoplasia type 2B
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q18553439)
(Q1553018)
(Q55785849)
(Q55788491)
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| (P1692) |
258.03
237.4
|
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| (P1748) |
C3227
|
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| (P1995) |
(Q162606)
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| (P2293) |
(Q18253720)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_10016
http://identifiers.org/doid/DOID:10016
http://www.orpha.net/ORDO/Orphanet_247709 http://www.orpha.net/ORDO/Orphanet_653 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
MEN type IIB MEN2B Multiple endocrine neoplasia, type 3 Wagenmann-Froboese syndrome mucosal neuroma syndrome multiple endocrine neoplasia type 2b Multiple Endocrine Neoplasia, Type Iii, Formerly Multiple Endocrine Neoplasia, Type III Multiple endocrine neoplasia, type 3 (formerly) Multiple endocrine neoplasia type 3 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B Neuromata, Mucosal, With Endocrine Tumors Multiple Endocrine Adenomatosis Type IIB Multiple Endocrine Neoplasia Type IIB MEN IIB Men 2B MEN Type 2B Multiple Endocrine Neoplasia Type III |
| description | autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities |
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