Source: ALL
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: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 2 9.1E-02 0 0
CUI: C0205815
Disease: Leiomyosarcoma, Epithelioid
Leiomyosarcoma, Epithelioid 		11 0 2 8.7E-02 0 0
CUI: C4551715
Disease: Pigmentary retinopathy
Pigmentary retinopathy 		11 0 2 8.7E-02 0 0
CUI: C0205816
Disease: Leiomyosarcoma, Myxoid
Leiomyosarcoma, Myxoid 		14 0 2 7.7E-02 0 0
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory 		14 0 2 7.7E-02 0 0
CUI: C0334606
Disease: Fibrous Meningioma
Fibrous Meningioma 		15 0 2 7.4E-02 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 7.1E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 7.1E-02 0 0
CUI: C0178272
Disease: Disorder of pulmonary circulation
Disorder of pulmonary circulation 		1 0 1 7.1E-02 0 0
CUI: C0231691
Disease: Cerebellar Gait Ataxia
Cerebellar Gait Ataxia 		1 0 1 7.1E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 7.1E-02 0 0
CUI: C0278161
Disease: Ataxia, Motor
Ataxia, Motor 		16 0 2 7.1E-02 0 0
CUI: C0343440
Disease: Pulmonary melioidosis
Pulmonary melioidosis 		1 0 1 7.1E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 7.1E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 7.1E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 7.1E-02 0 0
CUI: C0751836
Disease: Gait Ataxia, Sensory
Gait Ataxia, Sensory 		1 0 1 7.1E-02 0 0
CUI: C1266176
Disease: Atypical choroid plexus papilloma
Atypical choroid plexus papilloma 		1 0 1 7.1E-02 0 0
CUI: C1282522
Disease: Gastric Xanthoma
Gastric Xanthoma 		1 0 1 7.1E-02 0 0
CUI: C1333100
Disease: Squamous cell carcinoma of colon
Squamous cell carcinoma of colon 		1 0 1 7.1E-02 0 0
CUI: C1565106
Disease: Headache Disorders, Primary
Headache Disorders, Primary 		1 0 1 7.1E-02 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 7.1E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 7.1E-02 0 0
CUI: C2675336
Disease: Duplication 15q11-q13 Syndrome
Duplication 15q11-q13 Syndrome 		1 0 1 7.1E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 7.1E-02 0 0