DisGeNET - a database of gene-disease associations

Gene: PPARGC1A ×

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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:	10891
Gene Symbol:	PPARGC1A

PPARGC1A

CUI:	C0010308
Disease:	Congenital Hypothyroidism

Congenital Hypothyroidism

0.200

Biomarker

RGD

Evidence of a bigenomic regulation of mitochondrial gene expression by thyroid hormone during rat brain development.

2010