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Disease association ontology term - MONDO:0005217 - familial cardiomyopathy

Term summary

ID
MONDO:0005217
Name
familial cardiomyopathy
Ontology or CV name
Disease association
Definition
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:8000015 - 46,XY sex reversal 11

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

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MONDO:0009026 - Costello syndrome

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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: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:0009282 - multiple acyl-CoA dehydrogenase deficiency

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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:0008685 - Wolff-Parkinson-White syndrome

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