Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients. 20031356

2010
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR Genotype-phenotype correlation in Brazillian Rett syndrome patients. 19722030

2009
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR Homozygosity for MECP2 gene in a girl with classical Rett syndrome. 17881312

2008
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome. 17089071

2007
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR Prenatal diagnosis in Rett syndrome. 12065946

2003
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 GeneticVariation CLINVAR Chronic osteomyelitis in patients with sickle cell disease. 10944834

2000
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.190 CausalMutation CLINVAR