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: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 5.3E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 5.3E-02 0 0
CUI: C0268645
Disease: Cystinuria, type 3
Cystinuria, type 3 		1 0 1 5.3E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 5.3E-02 0 0
CUI: C0477611
Disease: [X]Spinal osteochondrosis, unspecified
[X]Spinal osteochondrosis, unspecified 		1 0 1 5.3E-02 0 0
CUI: C0597966
Disease: Juxtaglomerular cell hyperplasia
Juxtaglomerular cell hyperplasia 		1 0 1 5.3E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 5.3E-02 0 0
CUI: C0745150
Disease: Hypoglycemia, acute
Hypoglycemia, acute 		1 0 1 5.3E-02 0 0
CUI: C0751343
Disease: Myelitis, Postinfectious
Myelitis, Postinfectious 		1 0 1 5.3E-02 0 0
CUI: C0856247
Disease: Lumbar spine degeneration
Lumbar spine degeneration 		1 0 1 5.3E-02 0 0
CUI: C0861156
Disease: Visual phenomena
Visual phenomena 		1 0 1 5.3E-02 0 0
CUI: C0948755
Disease: Pulmonary failure
Pulmonary failure 		1 0 1 5.3E-02 0 0
CUI: C1321580
Disease: Trichobezoar disorder
Trichobezoar disorder 		1 0 1 5.3E-02 0 0
CUI: C1843315
Disease: Neuronopathy, Distal Hereditary Motor, Type Viib
Neuronopathy, Distal Hereditary Motor, Type Viib 		1 0 1 5.3E-02 0 0
CUI: C1843791
Disease: CARDIOMYOPATHY, DILATED, 1N
CARDIOMYOPATHY, DILATED, 1N 		1 0 1 5.3E-02 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 11 1 5.3E-02 10 6.6E-02
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 5.3E-02 0 0
CUI: C1857388
Disease: Cystinuria, Type A
Cystinuria, Type A 		1 0 1 5.3E-02 0 0
CUI: C1862554
Disease: COLTON-NULL PHENOTYPE
COLTON-NULL PHENOTYPE 		1 0 1 5.3E-02 0 0
CUI: C1866008
Disease: Muscular Dystrophy, Limb-Girdle, Type 2G
Muscular Dystrophy, Limb-Girdle, Type 2G 		1 0 1 5.3E-02 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 5.3E-02 0 0
CUI: C2930849
Disease: Von willebrand factor, deficiency
Von willebrand factor, deficiency 		1 0 1 5.3E-02 0 0
CUI: C2930900
Disease: Beta-sarcoglycanopathy
Beta-sarcoglycanopathy 		1 0 1 5.3E-02 0 0
CUI: C3160931
Disease: Ventricular dyssynchrony
Ventricular dyssynchrony 		1 0 1 5.3E-02 0 0
CUI: C3280674
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3 		1 0 1 5.3E-02 0 0