Source: CURATED ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome 		1 0 1 3.3E-03 0 0
CUI: C1150929
Disease: 2-oxo-hept-3-ene-1,7-dioate hydratase activity
2-oxo-hept-3-ene-1,7-dioate hydratase activity 		14 0 2 6.4E-03 0 0
CUI: C4304539
Disease: 20p12.3 microdeletion syndrome
20p12.3 microdeletion syndrome 		1 0 1 3.3E-03 0 0
CUI: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis 		11 0 1 3.2E-03 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2 		15 0 2 6.4E-03 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism 		8 0 1 3.3E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		3 0 1 3.3E-03 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		6 0 1 3.3E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 3.3E-03 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		33 0 3 9.1E-03 0 0
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye 		7 0 1 3.3E-03 0 0
CUI: C0744356
Disease: Abnormality of the genital system
Abnormality of the genital system 		3 0 1 3.3E-03 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 11 2.8E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		3 0 1 3.3E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		102 0 7 1.8E-02 0 0
CUI: C0234238
Disease: Ache
Ache 		49 0 4 1.2E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		6 0 1 3.3E-03 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 2 6.6E-03 0 0
CUI: C0702169
Disease: Acrania
Acrania 		28 0 2 6.1E-03 0 0
CUI: C0796147
Disease: Acrocallosal Syndrome
Acrocallosal Syndrome 		4 0 1 3.3E-03 0 0
CUI: C2931760
Disease: Acrocallosal syndrome, Schinzel type
Acrocallosal syndrome, Schinzel type 		3 0 1 3.3E-03 0 0
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia 		2 0 2 6.7E-03 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		16 0 3 9.6E-03 0 0
CUI: C2930971
Disease: Acroosteolysis dominant type
Acroosteolysis dominant type 		1 0 1 3.3E-03 0 0
CUI: C0751779
Disease: Action Myoclonus-Renal Failure Syndrome
Action Myoclonus-Renal Failure Syndrome 		18 0 1 3.2E-03 0 0