Preferred Name

NK2 HOMEOBOX 5

Synonyms

ATRIAL SEPTAL DEFECT 7 WITH ATRIOVENTRICULAR CONDUCTION DEFECTS

ID

http://purl.bioontology.org/ontology/OMIM/600584

altLabel

ATRIAL SEPTAL DEFECT 7 WITH ATRIOVENTRICULAR CONDUCTION DEFECTS

INTERRUPTED AORTIC ARCH

TETRALOGY OF FALLOT

NKX2.5, MOUSE, HOMOLOG OF

NKX2E

VENTRICULAR SEPTAL DEFECT 3

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS, SOMATIC

ATRIAL SEPTAL DEFECT 7 WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS

CSX1

CSX

DOUBLE-OUTLET RIGHT VENTRICLE

CARDIAC-SPECIFIC HOMEOBOX 1

TRUNCUS ARTERIOSUS

HYPOPLASTIC LEFT HEART SYNDROME 2

HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5

ATRIOVENTRICULAR SEPTAL DEFECT, SOMATIC

NKX2-5

NK2, DROSOPHILA, HOMOLOG OF, E

cui

C1413784

C0152419

C0039685

C4016679

C0013069

C0041206

C4016680

C1833590

C3280795

C2673630

C4016678

C3280785

Gene Locus

5q34

Gene Symbol

NKX2E

CHNG5

CSX

VSD3

HLHS2

NKX2-5

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/600584.0014

http://purl.bioontology.org/ontology/OMIM/600584.0013

http://purl.bioontology.org/ontology/OMIM/600584.0001

http://purl.bioontology.org/ontology/OMIM/600584.0018

http://purl.bioontology.org/ontology/OMIM/600584.0006

http://purl.bioontology.org/ontology/OMIM/600584.0007

http://purl.bioontology.org/ontology/OMIM/600584.0005

http://purl.bioontology.org/ontology/OMIM/600584.0019

http://purl.bioontology.org/ontology/OMIM/600584.0011

http://purl.bioontology.org/ontology/OMIM/600584.0022

http://purl.bioontology.org/ontology/OMIM/600584.0010

http://purl.bioontology.org/ontology/OMIM/600584.0016

http://purl.bioontology.org/ontology/OMIM/600584.0002

http://purl.bioontology.org/ontology/OMIM/600584.0023

http://purl.bioontology.org/ontology/OMIM/600584.0003

http://purl.bioontology.org/ontology/OMIM/600584.0024

http://purl.bioontology.org/ontology/OMIM/600584.0017

http://purl.bioontology.org/ontology/OMIM/600584.0015

http://purl.bioontology.org/ontology/OMIM/600584.0008

http://purl.bioontology.org/ontology/OMIM/600584.0004

http://purl.bioontology.org/ontology/OMIM/600584.0009

http://purl.bioontology.org/ontology/OMIM/600584.0021

http://purl.bioontology.org/ontology/OMIM/600584.0020

http://purl.bioontology.org/ontology/OMIM/600584.0012

MIMTYPEMEANING

Gene with known sequence

notation

600584

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

NK2 HOMEOBOX 5

tui

T028

T019

T033

T018

T047

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/Q25.21 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bmicc.cn/ontology/ICD10CN/Q21.3 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/LNC/LA19623-0 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/ICD10CM/Q21.3 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/ICD10/Q21.3 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bmicc.cn/ontology/ICD10CN/Q20.1 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://www.orpha.net/ORDO/Orphanet_123797 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/ICD10/Q20.1 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/MESH/D013771 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D004310 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D014338 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/ICD10CM/Q20.1 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/C567123 Medical Subject Headings / 医学主题词表 CUI