DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Macrocephaly ×

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:	8738
Gene Symbol:	CRADD

CRADD

CUI:	C0221355
Disease:	Macrocephaly

Macrocephaly

0.110

GeneticVariation

BEFREE

Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant.

2016

Entrez Id:	8738
Gene Symbol:	CRADD

CRADD

CUI:	C0221355
Disease:	Macrocephaly

Macrocephaly

0.110

Biomarker

HPO