Preferred Name | multiple endocrine neoplasia type 2B | |
Synonyms |
Wagenmann-Froboese syndrome Multiple endocrine neoplasia, type 3 MEN2B MEN type IIB mucosal neuroma syndrome |
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Definitions |
A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_10016 |
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Obsolete |
true |
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comment |
OMIM mapping confirmed by DO. [SN]. |
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alternative label |
Wagenmann-Froboese syndrome Multiple endocrine neoplasia, type 3 MEN2B MEN type IIB mucosal neuroma syndrome |
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database_cross_reference |
ICD9CM:258.03 MESH:D018814 SNOMEDCT_US_2023_03_01:61530001 ICD10CM:E31.23 UMLS_CUI:C0025269 ORDO:247709 OMIM:162300 NCI:C3227 |
|
definition |
A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. OMIM mapping confirmed by DO. [SN]. |
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has exact synonym |
Wagenmann-Froboese syndrome Multiple endocrine neoplasia, type 3 MEN2B MEN type IIB mucosal neuroma syndrome |
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has material basis in | ||
has_obo_namespace |
disease_ontology |
|
id |
DOID:10016 |
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in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
|
label |
multiple endocrine neoplasia type 2B |
|
notation |
DOID:10016 |
|
note |
A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. OMIM mapping confirmed by DO. [SN]. |
|
owl:deprecated |
true |
|
preferred label |
multiple endocrine neoplasia type 2B |
|
prefLabel |
multiple endocrine neoplasia type 2B |
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subClassOf |