Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10682
Gene Symbol: EBP
EBP
CUI: C4085243
Disease: MEND SYNDROME
MEND SYNDROME 		0.730 Biomarker GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308

2016
Entrez Id: 10682
Gene Symbol: EBP
EBP
CUI: C4085243
Disease: MEND SYNDROME
MEND SYNDROME 		0.730 Biomarker GENOMICS_ENGLAND A novel X-linked multiple congenital anomaly syndrome associated with an EBP mutation. 20949533

2010
Entrez Id: 10682
Gene Symbol: EBP
EBP
CUI: C4085243
Disease: MEND SYNDROME
MEND SYNDROME 		0.730 Biomarker GENOMICS_ENGLAND