Source: CLINVAR ×
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: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia 		2 11 2 1.00 1 7.7E-02
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		2 0 2 1.00 0 0
CUI: C1855739
Disease: Indifference to Pain, Congenital, Autosomal Recessive
Indifference to Pain, Congenital, Autosomal Recessive 		2 0 2 1.00 0 0
CUI: C2751778
Disease: Generalized Epilepsy With Febrile Seizures Plus, 7
Generalized Epilepsy With Febrile Seizures Plus, 7 		2 0 2 1.00 0 0
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B 		2 0 2 1.00 0 0
CUI: C4012054
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID 		2 0 2 1.00 0 0
CUI: C0344307
Disease: Absence of pain sensation
Absence of pain sensation 		3 0 2 0.67 0 0
CUI: C1867971
Disease: Acute episodes of neuropathic symptoms
Acute episodes of neuropathic symptoms 		3 0 2 0.67 0 0
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		4 0 2 0.50 0 0
CUI: C4023691
Disease: Abnormality of pain sensation
Abnormality of pain sensation 		4 0 2 0.50 0 0
CUI: C1858673
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 		2 0 1 0.33 0 0
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		2 0 1 0.33 0 0
CUI: C2751756
Disease: Febrile Convulsions, Familial, 3a
Febrile Convulsions, Familial, 3a 		2 0 1 0.33 0 0
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy 		3 0 1 0.25 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		3 0 1 0.25 0 0
CUI: C1301937
Disease: Talipes
Talipes 		3 0 1 0.25 0 0
CUI: C1843392
Disease: Death in childhood
Death in childhood 		3 0 1 0.25 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size 		3 0 1 0.25 0 0
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		3 0 1 0.25 0 0
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
Congenital Dysplasia Of The Hip 		3 0 1 0.25 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		4 0 1 0.20 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		4 0 1 0.20 0 0
CUI: C0431391
Disease: Hemimegalencephaly
Hemimegalencephaly 		5 0 1 0.17 0 0
CUI: C3805727
Disease: MEGALENCEPHALY, AUTOSOMAL DOMINANT
MEGALENCEPHALY, AUTOSOMAL DOMINANT 		6 0 1 0.14 0 0
CUI: C0241210
Disease: Speech Delay
Speech Delay 		11 0 1 8.3E-02 0 0