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Preferred Name

MENIN 1
Synonyms

ANGIOFIBROMA, SOMATIC
ID

http://purl.bioontology.org/ontology/OMIM/613733
altLabel

ANGIOFIBROMA, SOMATIC

MEN1

HYPERPARATHYROIDISM, FAMILIAL ISOLATED PRIMARY, MEN1 VARIANT

ADRENAL ADENOMA, SOMATIC

CARCINOID TUMOR OF LUNG

MENIN

MULTIPLE ENDOCRINE NEOPLASIA, TYPE I

LIPOMA, SOMATIC

HYPERPARATHYROIDISM, FAMILIAL ISOLATED PRIMARY

PARATHYROID ADENOMA, SOMATIC

MEN1 GENE
cui

C4551961

C2675664

C4017331

C0025267

C0280089

C0694884

C4017330

C4017332

C4479701
Gene Locus

11q13
Gene Symbol

MEN1
Has allelic variant

http://purl.bioontology.org/ontology/OMIM/613733.0007

http://purl.bioontology.org/ontology/OMIM/613733.0018

http://purl.bioontology.org/ontology/OMIM/613733.0019

http://purl.bioontology.org/ontology/OMIM/613733.0030

http://purl.bioontology.org/ontology/OMIM/613733.0001

http://purl.bioontology.org/ontology/OMIM/613733.0010

http://purl.bioontology.org/ontology/OMIM/613733.0035

http://purl.bioontology.org/ontology/OMIM/613733.0021

http://purl.bioontology.org/ontology/OMIM/613733.0022

http://purl.bioontology.org/ontology/OMIM/613733.0002

http://purl.bioontology.org/ontology/OMIM/613733.0003

http://purl.bioontology.org/ontology/OMIM/613733.0016

http://purl.bioontology.org/ontology/OMIM/613733.0014

http://purl.bioontology.org/ontology/OMIM/613733.0015

http://purl.bioontology.org/ontology/OMIM/613733.0034

http://purl.bioontology.org/ontology/OMIM/613733.0027

http://purl.bioontology.org/ontology/OMIM/613733.0004

http://purl.bioontology.org/ontology/OMIM/613733.0023

http://purl.bioontology.org/ontology/OMIM/613733.0008

http://purl.bioontology.org/ontology/OMIM/613733.0017

http://purl.bioontology.org/ontology/OMIM/613733.0009

http://purl.bioontology.org/ontology/OMIM/613733.0028

http://purl.bioontology.org/ontology/OMIM/613733.0031

http://purl.bioontology.org/ontology/OMIM/613733.0029

http://purl.bioontology.org/ontology/OMIM/613733.0020

http://purl.bioontology.org/ontology/OMIM/613733.0012

http://purl.bioontology.org/ontology/OMIM/613733.0011

http://purl.bioontology.org/ontology/OMIM/613733.0032

http://purl.bioontology.org/ontology/OMIM/613733.0025

http://purl.bioontology.org/ontology/OMIM/613733.0033

http://purl.bioontology.org/ontology/OMIM/613733.0005

http://purl.bioontology.org/ontology/OMIM/613733.0013

http://purl.bioontology.org/ontology/OMIM/613733.0024

http://purl.bioontology.org/ontology/OMIM/613733.0026

http://purl.bioontology.org/ontology/OMIM/613733.0006
MIMTYPEMEANING

Gene with known sequence
notation

613733
OMIM Entry Type

1
OMIM MimType Value

star
prefLabel

MENIN 1
tui

T191

T028

T033

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/E31.21 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI
http://purl.bioontology.org/ontology/MESH/C564166 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D018761 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/LNC/LP33138-6 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://www.orpha.net/ORDO/Orphanet_123196 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM