Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.600 Biomarker GENOMICS_ENGLAND Recently, a homozygous missense mutation in MED13L was found in two siblings with non-syndromic ID from a consanguineous family. 23403903

2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.600 Biomarker GENOMICS_ENGLAND Recently, a homozygous missense mutation in MED13L was found in two siblings with non-syndromic ID from a consanguineous family. 23403903

2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.600 Biomarker CTD_human Deep sequencing reveals 50 novel genes for recessive cognitive disorders. 21937992

2011