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: C3277849
Disease: 17,20-Lyase Deficiency, Isolated
17,20-Lyase Deficiency, Isolated 		1 0 1 2.0E-03 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome 		1 0 1 2.0E-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 1 1.9E-03 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		10 0 1 1.9E-03 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		9 0 1 1.9E-03 0 0
CUI: C0342471
Disease: 3 beta-Hydroxysteroid dehydrogenase deficiency
3 beta-Hydroxysteroid dehydrogenase deficiency 		1 0 1 2.0E-03 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism 		8 0 2 3.9E-03 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine 		9 0 1 1.9E-03 0 0
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		3 0 2 3.9E-03 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		16 0 3 5.8E-03 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 2.0E-03 0 0
CUI: C4022810
Disease: Abnormality of nervous system morphology
Abnormality of nervous system morphology 		10 0 1 1.9E-03 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		33 0 2 3.7E-03 0 0
CUI: C4025871
Disease: Abnormality of the face
Abnormality of the face 		9 0 1 1.9E-03 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue 		0 2 0 0 1 4.9E-03
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 9 1.5E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		102 0 9 1.5E-02 0 0
CUI: C0268603
Disease: Acetyl-CoA: carboxylase deficiency
Acetyl-CoA: carboxylase deficiency 		1 0 1 2.0E-03 0 0
CUI: C0234238
Disease: Ache
Ache 		49 0 4 7.2E-03 0 0
CUI: C3900122
Disease: Acid-Labile Subunit Deficiency
Acid-Labile Subunit Deficiency 		1 0 1 2.0E-03 0 0
CUI: C0001122
Disease: Acidosis
Acidosis 		2 0 1 2.0E-03 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		3 0 1 2.0E-03 0 0
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0 526 0 0 1 1.4E-03
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 1 2.0E-03 0 0
CUI: C0751449
Disease: Acquired Polyneuropathy
Acquired Polyneuropathy 		3 0 1 2.0E-03 0 0