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: C0238637
Disease: Anal pain
Anal pain 		1 0 1 1.00 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 1.00 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 1.00 0 0
CUI: C4553071
Disease: Anal Pain, CTCAE 5
Anal Pain, CTCAE 5 		1 0 1 1.00 0 0
CUI: C0037650
Disease: Somatoform Disorder
Somatoform Disorder 		2 0 1 0.50 0 0
CUI: C0234241
Disease: Indifference to pain
Indifference to pain 		2 0 1 0.50 0 0
CUI: C2751778
Disease: Generalized Epilepsy With Febrile Seizures Plus, 7
Generalized Epilepsy With Febrile Seizures Plus, 7 		2 0 1 0.50 0 0
CUI: C3151229
Disease: FEBRILE SEIZURES, FAMILIAL, 3B
FEBRILE SEIZURES, FAMILIAL, 3B 		2 0 1 0.50 0 0
CUI: C4012054
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID 		2 0 1 0.50 0 0
CUI: C4552061
Disease: Mandibular pain
Mandibular pain 		2 0 1 0.50 0 0
CUI: C0037140
Disease: B Virus Infection
B Virus Infection 		3 0 1 0.33 0 0
CUI: C0853946
Disease: Pain worsened
Pain worsened 		3 0 1 0.33 0 0
CUI: C1867971
Disease: Acute episodes of neuropathic symptoms
Acute episodes of neuropathic symptoms 		4 0 1 0.25 0 0
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		4 0 1 0.25 0 0
CUI: C0432262
Disease: Dysosteosclerosis
Dysosteosclerosis 		5 0 1 0.20 0 0
CUI: C1846620
Disease: Hemiclonic seizures
Hemiclonic seizures 		5 0 1 0.20 0 0
CUI: C2752089
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIA
Neuropathy, Hereditary Sensory And Autonomic, Type IIA 		5 0 1 0.20 0 0
CUI: C0151934
Disease: Hypogeusia
Hypogeusia 		6 0 1 0.17 0 0
CUI: C0236000
Disease: Jaw pain
Jaw pain 		6 0 1 0.17 0 0
CUI: C4023691
Disease: Abnormality of pain sensation
Abnormality of pain sensation 		6 0 1 0.17 0 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis 		6 0 1 0.17 0 0
CUI: C4552662
Disease: Rhinorrhea, CTCAE
Rhinorrhea, CTCAE 		6 0 1 0.17 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia 		7 0 1 0.14 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		7 0 1 0.14 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		8 0 1 0.12 0 0