Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.430 Biomarker disease PSYGENET Therefore, UFD1L may participate in the core cognitive deficits observed in schizophrenia. 23623450 2013
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.430 Biomarker disease PSYGENET A family- and population-based study of the UFD1L gene for schizophrenia. 18270977 2008
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.330 ChromosomalRearrangement disease ORPHANET
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		0.320 ChromosomalRearrangement disease ORPHANET
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		0.320 ChromosomalRearrangement disease ORPHANET
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.300 Biomarker group CTD_human A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. 10024240 1999
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.300 Biomarker group CTD_human A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. 10024240 1999
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association 		0.300 ChromosomalRearrangement disease ORPHANET
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME 		0.300 ChromosomalRearrangement disease ORPHANET
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		0.300 ChromosomalRearrangement disease ORPHANET