Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024
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

ID

http://purl.bioontology.org/ontology/OMIM/162300

altLabel

NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS

MEN2B

MUCOSAL NEUROMA SYNDROME

MEN IIB

MEN3, FORMERLY

WAGENMANN-FROBOESE SYNDROME

MULTIPLE ENDOCRINE NEOPLASIA, TYPE III, FORMERLY

cui

C0025269

Gene Locus

10q11.2

Gene Symbol

MEN2A

RET

HSCR1

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU016734

http://purl.bioontology.org/ontology/OMIM/MTHU000191

http://purl.bioontology.org/ontology/OMIM/MTHU003653

http://purl.bioontology.org/ontology/OMIM/MTHU016248

http://purl.bioontology.org/ontology/OMIM/MTHU000197

http://purl.bioontology.org/ontology/OMIM/MTHU008370

http://purl.bioontology.org/ontology/OMIM/MTHU016739

http://purl.bioontology.org/ontology/OMIM/MTHU016736

http://purl.bioontology.org/ontology/OMIM/MTHU000185

http://purl.bioontology.org/ontology/OMIM/MTHU016740

http://purl.bioontology.org/ontology/OMIM/MTHU016733

http://purl.bioontology.org/ontology/OMIM/MTHU001465

http://purl.bioontology.org/ontology/OMIM/MTHU016247

http://purl.bioontology.org/ontology/OMIM/MTHU041402

http://purl.bioontology.org/ontology/OMIM/MTHU016735

http://purl.bioontology.org/ontology/OMIM/MTHU016743

http://purl.bioontology.org/ontology/OMIM/MTHU001907

http://purl.bioontology.org/ontology/OMIM/MTHU000226

http://purl.bioontology.org/ontology/OMIM/MTHU015990

http://purl.bioontology.org/ontology/OMIM/MTHU001148

http://purl.bioontology.org/ontology/OMIM/MTHU000681

http://purl.bioontology.org/ontology/OMIM/MTHU000036

http://purl.bioontology.org/ontology/OMIM/MTHU010647

http://purl.bioontology.org/ontology/OMIM/MTHU015027

http://purl.bioontology.org/ontology/OMIM/MTHU016742

http://purl.bioontology.org/ontology/OMIM/MTHU000335

http://purl.bioontology.org/ontology/OMIM/MTHU003604

http://purl.bioontology.org/ontology/OMIM/MTHU016249

http://purl.bioontology.org/ontology/OMIM/MTHU016737

http://purl.bioontology.org/ontology/OMIM/MTHU001062

http://purl.bioontology.org/ontology/OMIM/MTHU003212

http://purl.bioontology.org/ontology/OMIM/MTHU016741

http://purl.bioontology.org/ontology/OMIM/MTHU016245

http://purl.bioontology.org/ontology/OMIM/MTHU016738

http://purl.bioontology.org/ontology/OMIM/MTHU010296

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

162300

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB

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]

tui

T191

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