Cardiomyopathy (Phenotype)

Synonyms:Disease of the heart muscle

Id:HP:0001638

Description:A myocardial disorder in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality.

Results found

Linked to

	Label	Description
	RPS4Y1 Gene (Entity type)	ribosomal protein S4 Y-linked 1
	CA2 Gene (Entity type)	carbonic anhydrase 2
	DLK1 Gene (Entity type)	delta like non-canonical Notch ligand 1
	ID1 Gene (Entity type)	inhibitor of DNA binding 1
	MAGEA6 Gene (Entity type)	MAGE family member A6
	FABP4 Gene (Entity type)	fatty acid binding protein 4
	TFF1 Gene (Entity type)	trefoil factor 1
	HBB Gene (Entity type)	hemoglobin subunit beta
	KRT5 Gene (Entity type)	keratin 5
	KIF20A Gene (Entity type)	kinesin family member 20A

RPS4Y1

Gene (Entity type)

ribosomal protein S4 Y-linked 1

CA2

Gene (Entity type)

carbonic anhydrase 2

DLK1

Gene (Entity type)

delta like non-canonical Notch ligand 1

ID1

Gene (Entity type)

inhibitor of DNA binding 1

MAGEA6

Gene (Entity type)

MAGE family member A6

FABP4

Gene (Entity type)

fatty acid binding protein 4

TFF1

Gene (Entity type)

trefoil factor 1

HBB

Gene (Entity type)

hemoglobin subunit beta

KRT5

Gene (Entity type)

keratin 5

KIF20A

Gene (Entity type)

kinesin family member 20A

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@CFDE Workbench 2025

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2025