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Disease association ontology term - MONDO:0024573 - familial hypertrophic cardiomyopathy

Term summary

ID
MONDO:0024573
Name
familial hypertrophic cardiomyopathy
Ontology or CV name
Disease association
Definition
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.

Parents

Annotation

Disease association

MONDO:8000015 - 46,XY sex reversal 11

References:

Genes:

MONDO:0015280 - cardiofaciocutaneous syndrome

References:

Genes:

MONDO:0007265 - cardiofaciocutaneous syndrome 1

References:

Genes:

MONDO:0014112 - cardiofaciocutaneous syndrome 2

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Genes:

MONDO:0014113 - cardiofaciocutaneous syndrome 3

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Genes:

MONDO:0014114 - cardiofaciocutaneous syndrome 4

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Genes:

MONDO:0012557 - cardiomyopathy-hypotonia-lactic acidosis syndrome

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Genes:

MONDO:0009026 - Costello syndrome

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Genes:

MONDO:0008647 - hypertrophic cardiomyopathy 1

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Genes:

MONDO:0012112 - hypertrophic cardiomyopathy 10

References:

Genes:

MONDO:0012799 - hypertrophic cardiomyopathy 11

References:

Genes:

MONDO:0013197 - hypertrophic cardiomyopathy 14

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Genes:

MONDO:0010946 - hypertrophic cardiomyopathy 6

References:

Genes:

MONDO:0012111 - hypertrophic cardiomyopathy 8

References:

Genes:

MONDO:0009282 - multiple acyl-CoA dehydrogenase deficiency

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Genes:

MONDO:0018997 - Noonan syndrome

References:

Genes:

MONDO:0033669 - Noonan syndrome 13

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Genes:

MONDO:0012371 - Noonan syndrome 3

References:

Genes:

MONDO:0013186 - Noonan syndrome 6

References:

Genes:

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

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Genes: