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: C0029307
Disease: Oroya Fever
Oroya Fever 		1 0 1 6.2E-02 0 0
CUI: C0275584
Disease: Cutaneous nocardiosis
Cutaneous nocardiosis 		1 0 1 6.2E-02 0 0
CUI: C0393560
Disease: Vascular Dementia, Acute Onset
Vascular Dementia, Acute Onset 		1 0 1 6.2E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 6.2E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 6.2E-02 0 0
CUI: C0524679
Disease: Neuropapillitis
Neuropapillitis 		1 0 1 6.2E-02 0 0
CUI: C0559523
Disease: Genital tuberculosis
Genital tuberculosis 		1 0 1 6.2E-02 0 0
CUI: C0600359
Disease: Arteriosclerotic Dementia
Arteriosclerotic Dementia 		1 0 1 6.2E-02 0 0
CUI: C1332860
Disease: Cauda Equina Paraganglioma
Cauda Equina Paraganglioma 		1 0 1 6.2E-02 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 6.2E-02 0 0
CUI: C1838876
Disease: MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE
MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE 		1 0 1 6.2E-02 0 0
CUI: C1854467
Disease: Spastic paraplegia 13, autosomal dominant
Spastic paraplegia 13, autosomal dominant 		1 0 1 6.2E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 6.2E-02 0 0
CUI: C2749936
Disease: SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 6.2E-02 0 0
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		1 0 1 6.2E-02 0 0
CUI: C3276074
Disease: PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS 		1 0 1 6.2E-02 0 0
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		1 0 1 6.2E-02 0 0
CUI: C3532243
Disease: Fatal infantile mitochondrial cardiomyopathy
Fatal infantile mitochondrial cardiomyopathy 		1 0 1 6.2E-02 0 0
CUI: C3539494
Disease: SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE 		1 0 1 6.2E-02 0 0
CUI: C3553656
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB 		1 0 1 6.2E-02 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 6.2E-02 0 0
CUI: C4021255
Disease: Weakness due to upper motor neuron dysfunction
Weakness due to upper motor neuron dysfunction 		1 0 1 6.2E-02 0 0
CUI: C4021807
Disease: Abnormality of the auditory canal
Abnormality of the auditory canal 		1 0 1 6.2E-02 0 0
CUI: C4022005
Disease: Carotid paraganglioma
Carotid paraganglioma 		1 0 1 6.2E-02 0 0
CUI: C4073166
Disease: Abnormality of jaw muscles
Abnormality of jaw muscles 		1 0 1 6.2E-02 0 0