DisGeNET - a database of gene-disease associations

Source: INFERRED

Disease: Severe global developmental delay ×

Gene: MECP2 ×

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:	4204
Gene Symbol:	MECP2

MECP2

CUI:	C1837397
Disease:	Severe global developmental delay

Severe global developmental delay

0.100

CausalMutation

CLINVAR

Entrez Id:	4204
Gene Symbol:	MECP2

MECP2

CUI:	C1837397
Disease:	Severe global developmental delay

Severe global developmental delay

0.100

Biomarker

HPO