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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/162300
http://purl.bioontology.org/ontology/OMIM/162300
|
|---|---|
| Preferred Name | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB |
| Synonyms |
NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS
MEN2B
MUCOSAL NEUROMA SYNDROME
MEN IIB
MEN3, FORMERLY
WAGENMANN-FROBOESE SYNDROME
MULTIPLE ENDOCRINE NEOPLASIA, TYPE III, FORMERLY
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS
MEN2B
MUCOSAL NEUROMA SYNDROME
MEN IIB
MEN3, FORMERLY
WAGENMANN-FROBOESE SYNDROME
MULTIPLE ENDOCRINE NEOPLASIA, TYPE III, FORMERLY
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|---|---|
| prefLabel | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB
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| Gene Symbol |
MEN2A
RET
HSCR1
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| Scope Statement | Caused by mutation in the RET protooncogene (RET, 164761.0013) [MOLECULAR BASIS]
Fifty percent of cases are sporadic [MISCELLANEOUS]
Medullary thyroid cancer is aggressive and can occur in childhood [MISCELLANEOUS]
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| type | |
| Has manifestation |
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| tui | T191
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| Gene Locus | 10q11.2
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| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 162300
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| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C0025269
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| OMIM Entry Type | 3
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| OMIM MimType Value | pound
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| Delete | Subject | Author | Type | Created |
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