DisGeNET - a database of gene-disease associations

Source: CTD_human

Disease: Hypertrophic Cardiomyopathy ×

Gene: POMC ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	5443
Gene Symbol:	POMC

POMC

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.300

Biomarker

CTD_human

[Hypertrophic myocardiopathy during the corticotropin treatment of infantile spasms].

8928979

1996

Entrez Id:	5443
Gene Symbol:	POMC

POMC

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.300

Biomarker

CTD_human

Hypertrophic cardiomyopathy during corticotropin therapy for infantile spasms. A clinical and echocardiographic study.

8381257

1993

Entrez Id:	5443
Gene Symbol:	POMC

POMC

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.300

Biomarker

CTD_human

[Secondary diseases of the heart muscle and their differential diagnosis in childhood].

2536513

1989

Entrez Id:	5443
Gene Symbol:	POMC

POMC

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.300

Biomarker

CTD_human

[Hypertrophic cardiomyopathy induced by ACTH].

2831920

1988

Entrez Id:	5443
Gene Symbol:	POMC

POMC

CUI:	C0007194
Disease:	Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy

0.300

Biomarker

CTD_human

[Secondary myocardial hypertrophy in newborn infants and infants without congenital heart defect].

2853496

1988