Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Undifferentiated somatoform disorder
1 0 1 0.17 0 0
Respiratory distress syndrome, children
1 0 1 0.17 0 0
CUI: C0745031
Disease: homicidal
homicidal
1 0 1 0.17 0 0
CUI: C0751445
Disease: Encephalitis, Polio
Encephalitis, Polio
1 0 1 0.17 0 0
CUI: C0751446
Disease: Poliomyelitis, Nonpoliovirus
Poliomyelitis, Nonpoliovirus
1 0 1 0.17 0 0
CUI: C0751447
Disease: Poliomyelitis, Preparalytic
Poliomyelitis, Preparalytic
1 0 1 0.17 0 0
CUI: C1527258
Disease: Infantile paralysis
Infantile paralysis
1 0 1 0.17 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome
1 0 1 0.17 0 0
Multiminicore Disease, Moderate, with Hand Involvement
1 0 1 0.17 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy
1 0 1 0.17 0 0
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
1 0 1 0.17 0 0
Malignant hyperthermia susceptibility type 1
1 0 1 0.17 0 0
CUI: C3553358
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 3
COENZYME Q10 DEFICIENCY, PRIMARY, 3
1 0 1 0.17 0 0
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4
1 0 1 0.17 0 0
CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
1 0 1 0.17 0 0
CUI: C4021030
Disease: Type III lissencephaly
Type III lissencephaly
1 0 1 0.17 0 0
CUI: C4476998
Disease: Frog-leg posture
Frog-leg posture
1 0 1 0.17 0 0
Congenital myopathy with myasthenic-like onset
1 0 1 0.17 0 0
CUI: C4724572
Disease: Obstructive apnea
Obstructive apnea
1 0 1 0.17 0 0
Benign Samaritan congenital myopathy
1 0 1 0.17 0 0
CUI: C0031880
Disease: Obesity Hypoventilation Syndrome
Obesity Hypoventilation Syndrome
2 0 1 0.14 0 0
CUI: C0155338
Disease: Total ophthalmoplegia
Total ophthalmoplegia
2 0 1 0.14 0 0
Exertional rhabdomyolysis (disorder)
2 0 1 0.14 0 0
CUI: C0340756
Disease: Stenosis, Pulmonary Vein
Stenosis, Pulmonary Vein
2 0 1 0.14 0 0
CUI: C0392375
Disease: despondency
despondency
2 0 1 0.14 0 0