YY1, YY1 transcription factor, 7528

N. diseases: 245; N. variants: 10
Disease: GABRIELE-DE VRIES SYNDROME ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 GermlineCausalMutation disease ORPHANET YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. 28575647 2017
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 GeneticVariation disease UNIPROT YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. 28575647 2017
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 Biomarker disease GENOMICS_ENGLAND YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. 28575647 2017
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 Biomarker disease GENOMICS_ENGLAND YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. 28575647 2017
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 Biomarker disease GENOMICS_ENGLAND YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. 28575647 2017
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 GeneticVariation disease UNIPROT A de novo paradigm for mental retardation. 21076407 2010
CUI: C4479652
Disease: GABRIELE-DE VRIES SYNDROME
GABRIELE-DE VRIES SYNDROME 		0.700 CausalMutation disease CLINVAR