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: C0033132
Disease: Cerebellar Degenerations, Primary
Cerebellar Degenerations, Primary 		1 0 1 2.3E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 2.3E-02 0 0
CUI: C0270755
Disease: Corticostriatal-Spinal Degeneration
Corticostriatal-Spinal Degeneration 		1 0 1 2.3E-02 0 0
CUI: C0272256
Disease: Solitary Osseous Plasmacytoma
Solitary Osseous Plasmacytoma 		1 0 1 2.3E-02 0 0
CUI: C0278685
Disease: Stage I Ovarian Cancer AJCC v6 and v7
Stage I Ovarian Cancer AJCC v6 and v7 		1 0 1 2.3E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 2.3E-02 0 0
CUI: C0333814
Disease: Pappenheimer body (morphologic abnormality)
Pappenheimer body (morphologic abnormality) 		1 0 1 2.3E-02 0 0
CUI: C0334483
Disease: Adult rhabdomyoma
Adult rhabdomyoma 		1 0 1 2.3E-02 0 0
CUI: C0398562
Disease: Triose phosphate isomerase deficiency
Triose phosphate isomerase deficiency 		1 0 1 2.3E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 2.3E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 2.3E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 2.3E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 2.3E-02 0 0
CUI: C0742608
Disease: colon (non-specific) polyp hyperplastic
colon (non-specific) polyp hyperplastic 		1 0 1 2.3E-02 0 0
CUI: C0796028
Disease: ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION 		1 0 1 2.3E-02 0 0
CUI: C1335748
Disease: Renal Pelvis Adenocarcinoma
Renal Pelvis Adenocarcinoma 		1 0 1 2.3E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.3E-02 0 0
CUI: C1834692
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA 		1 0 1 2.3E-02 0 0
CUI: C1836155
Disease: Myopathy, Myofibrillar, Zasp-Related
Myopathy, Myofibrillar, Zasp-Related 		1 0 1 2.3E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 2.3E-02 0 0
CUI: C1839566
Disease: CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5 		1 0 1 2.3E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 2.3E-02 0 0
CUI: C1842137
Disease: Nonsyndromic sensorineural hearing loss
Nonsyndromic sensorineural hearing loss 		1 0 1 2.3E-02 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 2.3E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 2.3E-02 0 0