DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Polydactyly, preaxial 4 ×

Gene: GLI3 ×

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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:	2737
Gene Symbol:	GLI3

GLI3

CUI:	C1868111
Disease:	Polydactyly, preaxial 4

Polydactyly, preaxial 4

0.700

GermlineCausalMutation

ORPHANET

Nosology and classification of genetic skeletal disorders: 2015 revision.

2015