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: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3
2 14 2 0.50 10 2.5E-02
CUI: C2751756
Disease: Febrile Convulsions, Familial, 3a
Febrile Convulsions, Familial, 3a
2 0 2 0.50 0 0
Generalized Epilepsy With Febrile Seizures Plus, 7
2 0 2 0.50 0 0
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B
2 0 2 0.50 0 0
CUI: C3698357
Disease: Refractory myoclonic epilepsy
Refractory myoclonic epilepsy
2 0 2 0.50 0 0
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
2 0 2 0.50 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size
3 2 2 0.40 1 2.5E-03
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
4 58 2 0.33 28 6.6E-02
Acute episodes of neuropathic symptoms
4 0 2 0.33 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures
5 0 2 0.29 0 0
Neuropathy, Hereditary Sensory And Autonomic, Type IIA
5 0 2 0.29 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells
1 0 1 0.25 0 0
CUI: C0238637
Disease: Anal pain
Anal pain
1 0 1 0.25 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain
1 0 1 0.25 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia
1 0 1 0.25 0 0
Refractory juvenile myoclonic epilepsy
1 0 1 0.25 0 0
CUI: C3805727
Disease: MEGALENCEPHALY, AUTOSOMAL DOMINANT
MEGALENCEPHALY, AUTOSOMAL DOMINANT
6 0 2 0.25 0 0
Sudden Unexplained Death in Childhood
1 0 1 0.25 0 0
CUI: C4023691
Disease: Abnormality of pain sensation
Abnormality of pain sensation
6 0 2 0.25 0 0
CUI: C4553071
Disease: Anal Pain, CTCAE 5
Anal Pain, CTCAE 5
1 0 1 0.25 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia
7 0 2 0.22 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER
13 0 3 0.21 0 0
CUI: C0037650
Disease: Somatoform Disorder
Somatoform Disorder
2 0 1 0.20 0 0
CUI: C0234241
Disease: Indifference to pain
Indifference to pain
2 0 1 0.20 0 0
CUI: C0338478
Disease: Idiopathic Myoclonic Epilepsy
Idiopathic Myoclonic Epilepsy
8 0 2 0.20 0 0