Source: CLINVAR ×
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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		237 0 2 8.0E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		13 0 1 3.8E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 1 3.3E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		15 0 1 3.6E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 1.5E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 1 1.8E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		15 0 1 3.6E-02 0 0
CUI: C0008489
Disease: Chorea
Chorea 		11 0 1 4.2E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 0 2 4.3E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		31 0 1 2.3E-02 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		7 0 1 5.0E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling 		14 0 2 7.7E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		34 0 1 2.1E-02 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		9 0 1 4.5E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 2.2E-02 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		10 0 1 4.3E-02 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		3 0 1 6.2E-02 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis 		4 0 1 5.9E-02 0 0
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		63 0 1 1.3E-02 0 0
CUI: C0020649
Disease: Hypotension
Hypotension 		3 0 1 6.2E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		25 0 1 2.6E-02 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		4 0 1 5.9E-02 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		5 0 1 5.6E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		28 0 1 2.4E-02 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		39 0 1 1.9E-02 0 0