DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Thyroid Dyshormonogenesis 1 ×

Gene: DUOX2 ×

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:	50506
Gene Symbol:	DUOX2

DUOX2

CUI:	C1848805
Disease:	Thyroid Dyshormonogenesis 1

Thyroid Dyshormonogenesis 1

0.300

GermlineCausalMutation

ORPHANET

Genetic causes of congenital hypothyroidism due to dyshormonogenesis.

21543982

2011

Entrez Id:	50506
Gene Symbol:	DUOX2

DUOX2

CUI:	C1848805
Disease:	Thyroid Dyshormonogenesis 1

Thyroid Dyshormonogenesis 1

0.300

GermlineCausalMutation

ORPHANET

Congenital hypothyroidism.

20537182

2010