Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		0.730 GeneticVariation UNIPROT Mutations in MED12 cause X-linked Ohdo syndrome. 23395478

2013
Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		0.730 GermlineCausalMutation ORPHANET Mutations in MED12 cause X-linked Ohdo syndrome. 23395478

2013
Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		0.730 Biomarker GENOMICS_ENGLAND A form of X-linked mental retardation with marfanoid habitus. 6711603

1984
Entrez Id: 9968
Gene Symbol: MED12
MED12
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		0.730 Biomarker GENOMICS_ENGLAND