DisGeNET - a database of gene-disease associations

Source: CLINVAR

Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 ×

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:	2719
Gene Symbol:	GPC3

GPC3

CUI:	C0796154
Disease:	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1

SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1

1.000

CausalMutation

CLINVAR

Entrez Id:	2719
Gene Symbol:	GPC3

GPC3

CUI:	C0796154
Disease:	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1

SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1

1.000

GeneticVariation

CLINVAR