Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024
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Preferred Name

MULTIPLE ENDOCRINE NEOPLASIA, TYPE I
Synonyms

MEN1

MEN I

MEN1 SOMATIC MUTATIONS

MEA I

WERMER SYNDROME

ENDOCRINE ADENOMATOSIS, MULTIPLE
ID

http://purl.bioontology.org/ontology/OMIM/131100
altLabel

MEN1

MEN I

MEN1 SOMATIC MUTATIONS

MEA I

WERMER SYNDROME

ENDOCRINE ADENOMATOSIS, MULTIPLE
cui

C3149237

C0025267
Gene Locus

11q13
Gene Symbol

MEN1
Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU018354

http://purl.bioontology.org/ontology/OMIM/MTHU036718

http://purl.bioontology.org/ontology/OMIM/MTHU018355

http://purl.bioontology.org/ontology/OMIM/MTHU018342

http://purl.bioontology.org/ontology/OMIM/MTHU018348

http://purl.bioontology.org/ontology/OMIM/MTHU017039

http://purl.bioontology.org/ontology/OMIM/MTHU016150

http://purl.bioontology.org/ontology/OMIM/MTHU018352

http://purl.bioontology.org/ontology/OMIM/MTHU018350

http://purl.bioontology.org/ontology/OMIM/MTHU000371

http://purl.bioontology.org/ontology/OMIM/MTHU018346

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

http://purl.bioontology.org/ontology/OMIM/MTHU018337

http://purl.bioontology.org/ontology/OMIM/MTHU018340

http://purl.bioontology.org/ontology/OMIM/MTHU018353

http://purl.bioontology.org/ontology/OMIM/MTHU018341

http://purl.bioontology.org/ontology/OMIM/MTHU016145

http://purl.bioontology.org/ontology/OMIM/MTHU018339

http://purl.bioontology.org/ontology/OMIM/MTHU018344

http://purl.bioontology.org/ontology/OMIM/MTHU018347

http://purl.bioontology.org/ontology/OMIM/MTHU016146

http://purl.bioontology.org/ontology/OMIM/MTHU018343

http://purl.bioontology.org/ontology/OMIM/MTHU018336

http://purl.bioontology.org/ontology/OMIM/MTHU018345

http://purl.bioontology.org/ontology/OMIM/MTHU018349

http://purl.bioontology.org/ontology/OMIM/MTHU036717

http://purl.bioontology.org/ontology/OMIM/MTHU018338

http://purl.bioontology.org/ontology/OMIM/MTHU018351

http://purl.bioontology.org/ontology/OMIM/MTHU016246
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

131100
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

MULTIPLE ENDOCRINE NEOPLASIA, TYPE I
Scope Statement

Caused by mutation in the menin gene (MEN1, 613733.0001) [MOLECULAR BASIS]
tui

T033

T191
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRFRE/10073150 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRFRE/10027180 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10028194 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10073150 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10027180 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10026979 MEDDRA CUI
http://purl.bioontology.org/ontology/CSP/2009-6300 CRISP CUI
http://purl.bioontology.org/ontology/SNOMEDCT/30664006 SNOMEDCT CUI
http://purl.bioontology.org/ontology/MDRFRE/10028194 MDRFRE CUI
http://purl.bioontology.org/ontology/NDFRT/N0000003850 NDFRT CUI
http://purl.bioontology.org/ontology/MDRGER/10027180 MDRGER CUI
http://purl.bioontology.org/ontology/ICD10CM/E31.21 ICD10CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10026979 MDRFRE CUI
http://purl.bioontology.org/ontology/MESH/D018761 MESH CUI
http://purl.bioontology.org/ontology/MDRFRE/10028190 MDRFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/30664006 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10028190 MEDDRA CUI
http://purl.bioontology.org/ontology/MSHFRE/D018761 MSHFRE CUI
http://purl.bioontology.org/ontology/SNMI/DB-02110 SNMI CUI
http://purl.bioontology.org/ontology/PDQ/CDR0000654711 PDQ CUI
http://purl.bioontology.org/ontology/MDRGER/10026979 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10073150 MDRGER CUI
http://purl.bioontology.org/ontology/RCD/X40OZ RCD CUI
http://purl.bioontology.org/ontology/ICD9CM/258.01 ICD9CM CUI
http://purl.bioontology.org/ontology/MDRGER/10028190 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10028194 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10028194 MEDDRA LOOM