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: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis 		6 0 1 0.14 0 0
CUI: C4552662
Disease: Rhinorrhea, CTCAE
Rhinorrhea, CTCAE 		6 0 1 0.14 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia 		7 0 2 0.29 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		7 0 1 0.12 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		8 0 1 0.11 0 0
CUI: C0338478
Disease: Idiopathic Myoclonic Epilepsy
Idiopathic Myoclonic Epilepsy 		8 0 1 0.11 0 0
CUI: C0338479
Disease: Symptomatic Myoclonic Epilepsy
Symptomatic Myoclonic Epilepsy 		8 0 1 0.11 0 0
CUI: C0393695
Disease: Early Childhood Epilepsy, Myoclonic
Early Childhood Epilepsy, Myoclonic 		8 0 1 0.11 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		8 0 1 0.11 0 0
CUI: C0751120
Disease: Benign Infantile Myoclonic Epilepsy
Benign Infantile Myoclonic Epilepsy 		8 0 1 0.11 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury 		8 0 1 0.11 0 0
CUI: C1852289
Disease: Autoamputation of digits
Autoamputation of digits 		8 0 1 0.11 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration 		8 0 1 0.11 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 1.0E-01 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 1.0E-01 0 0
CUI: C0151827
Disease: Eye pain
Eye pain 		10 0 1 9.1E-02 0 0
CUI: C0393703
Disease: Myoclonic Absence Epilepsy
Myoclonic Absence Epilepsy 		10 0 1 9.1E-02 0 0
CUI: C1298685
Disease: Chronic pain syndrome
Chronic pain syndrome 		10 0 1 9.1E-02 0 0
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee 		10 0 1 9.1E-02 0 0
CUI: C0030578
Disease: Paronychia Inflammation
Paronychia Inflammation 		11 0 1 8.3E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets 		11 0 1 8.3E-02 0 0
CUI: C0438414
Disease: Myoclonic Encephalopathy
Myoclonic Encephalopathy 		11 0 1 8.3E-02 0 0
CUI: C0917800
Disease: Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile 		11 0 1 8.3E-02 0 0
CUI: C1844690
Disease: Limited knee extension
Limited knee extension 		11 0 1 8.3E-02 0 0
CUI: C4014430
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 		11 0 1 8.3E-02 0 0