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Disease association ontology term - MONDO:0005267 - heart disorder

Term summary

ID
MONDO:0005267
Name
heart disorder
Ontology or CV name
Disease association
Definition
A disease involving the heart and/or pericardium.

Parents

Annotation

Disease association

MONDO:0005267 - heart disorder

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Genes:

MONDO:8000015 - 46,XY sex reversal 11

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Genes:

MONDO:0014340 - atrial fibrillation, familial, 15

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MONDO:0015001 - atrial fibrillation, familial, 18

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MONDO:0013567 - atrial septal defect 3

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MONDO:0013011 - atrial septal defect 5

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MONDO:0013770 - atrial septal defect 9

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MONDO:0013769 - atrioventricular septal defect 5

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MONDO:0014558 - autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

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MONDO:0012728 - Brugada syndrome 2

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MONDO:0011451 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

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MONDO:0014051 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2

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MONDO:0014667 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3

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MONDO:0014668 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

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MONDO:0015280 - cardiofaciocutaneous syndrome

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MONDO:0007265 - cardiofaciocutaneous syndrome 1

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MONDO:0014112 - cardiofaciocutaneous syndrome 2

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MONDO:0014113 - cardiofaciocutaneous syndrome 3

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MONDO:0014114 - cardiofaciocutaneous syndrome 4

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MONDO:0032592 - cardiomyopathy, dilated, 2c

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MONDO:0030300 - cardiomyopathy, dilated, 2D

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MONDO:0859358 - cardiomyopathy, dilated, 2H

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MONDO:0957545 - cardiomyopathy, dilated, 2I

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MONDO:0030330 - cardiomyopathy, familial restrictive, 6

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MONDO:0012557 - cardiomyopathy-hypotonia-lactic acidosis syndrome

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MONDO:0013529 - catecholaminergic polymorphic ventricular tachycardia 3

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MONDO:0013966 - catecholaminergic polymorphic ventricular tachycardia 4

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MONDO:0010221 - CHIME syndrome

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MONDO:0012637 - COG1-congenital disorder of glycosylation

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MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant

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MONDO:0012011 - coronary artery disease, autosomal dominant, 1

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MONDO:0009026 - Costello syndrome

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MONDO:0005021 - dilated cardiomyopathy

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MONDO:0012808 - dilated cardiomyopathy 1AA

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MONDO:0013198 - dilated cardiomyopathy 1EE

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MONDO:0013339 - dilated cardiomyopathy 1GG

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MONDO:0014073 - dilated cardiomyopathy 1II

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MONDO:0013261 - dilated cardiomyopathy 1R

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MONDO:0013262 - dilated cardiomyopathy 1S

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MONDO:0012556 - DK1-congenital disorder of glycosylation

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MONDO:0015487 - fatal infantile encephalocardiomyopathy

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MONDO:0017694 - glycogen storage disease due to acid maltase deficiency, infantile onset

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MONDO:0018485 - glycogen storage disease due to acid maltase deficiency, late-onset

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MONDO:0009290 - glycogen storage disease II

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MONDO:0002869 - heart valve disorder

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MONDO:0005045 - hypertrophic cardiomyopathy

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MONDO:0008647 - hypertrophic cardiomyopathy 1

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MONDO:0012112 - hypertrophic cardiomyopathy 10

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MONDO:0012799 - hypertrophic cardiomyopathy 11

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MONDO:0013197 - hypertrophic cardiomyopathy 14

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MONDO:0010946 - hypertrophic cardiomyopathy 6

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MONDO:0012111 - hypertrophic cardiomyopathy 8

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MONDO:0009867 - lethal congenital glycogen storage disease of heart

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MONDO:0014976 - lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome

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MONDO:0032915 - long QT syndrome 16

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MONDO:0009282 - multiple acyl-CoA dehydrogenase deficiency

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MONDO:0032852 - myopathy, congenital, with structured cores and z-line abnormalities

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MONDO:0032853 - myopathy, distal, 6, adult-onset, autosomal dominant

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MONDO:0018997 - Noonan syndrome

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MONDO:0033669 - Noonan syndrome 13

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MONDO:0012371 - Noonan syndrome 3

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MONDO:0013186 - Noonan syndrome 6

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MONDO:0054588 - Noonan syndrome-like disorder with loose anagen hair 2

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MONDO:0013968 - PGM1-congenital disorder of glycosylation

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MONDO:0005201 - restrictive cardiomyopathy

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MONDO:0008922 - Sengers syndrome

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MONDO:0014784 - severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome

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MONDO:0859368 - short QT syndrome 7

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MONDO:0859173 - sick sinus syndrome 4

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MONDO:0010711 - TARP syndrome

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MONDO:0008542 - tetralogy of fallot

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MONDO:0014881 - transketolase deficiency

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MONDO:0013063 - ventricular fibrillation, paroxysmal familial, 2

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MONDO:0030077 - vertebral, cardiac, renal, and limb defects syndrome 3

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MONDO:0008685 - Wolff-Parkinson-White syndrome

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