DisGeNET - a database of gene-disease associations

Source: ALL

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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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0750929
Disease:	Arnold-Chiari Malformation, Type I

Arnold-Chiari Malformation, Type I

0.010

GeneticVariation

disease

BEFREE

Multiple marker analysis identified a risk haplotype for classical CMI in ALDH1A2 and CDX1.

2013