Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64324
Gene Symbol: NSD1
NSD1
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 AlteredExpression LHGDN We demonstrate that NUP98-NSD1 induces AML in vivo, sustains self-renewal of myeloid stem cells in vitro, and enforces expression of the HoxA7, HoxA9, HoxA10 and Meis1 proto-oncogenes. 17589499

2007
Entrez Id: 64324
Gene Symbol: NSD1
NSD1
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.440 GeneticVariation LHGDN Interestingly, mental retardation was consistently more severe in patients with NSD1 deletions. 12807965

2003
Entrez Id: 64324
Gene Symbol: NSD1
NSD1
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		0.430 Biomarker LHGDN Two 11p15 anomalies were identified in a series of 20 patients with Sotos syndrome, and two NSD1 mutations were identified in a series of 52 patients with BWS. 14997421

2004