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: C0006897
Disease: Capillariasis
Capillariasis 		1 0 1 0.50 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis 		1 0 1 0.50 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness 		1 0 1 0.50 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection 		1 0 1 0.50 0 0
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		1 0 1 0.50 0 0
CUI: C4016601
Disease: SIDEROBLASTIC ANEMIA, ACQUIRED IDIOPATHIC
SIDEROBLASTIC ANEMIA, ACQUIRED IDIOPATHIC 		1 0 1 0.50 0 0
CUI: C4016602
Disease: CYTOCHROME c OXIDASE I DEFICIENCY
CYTOCHROME c OXIDASE I DEFICIENCY 		1 0 1 0.50 0 0
CUI: C4022677
Disease: Female anorgasmia
Female anorgasmia 		1 0 1 0.50 0 0
CUI: C0009225
Disease: Coenuriasis
Coenuriasis 		2 0 1 0.33 0 0
CUI: C0036231
Disease: Sarcocystosis
Sarcocystosis 		2 0 1 0.33 0 0
CUI: C0086227
Disease: Enterobiasis
Enterobiasis 		2 0 1 0.33 0 0
CUI: C0749201
Disease: Orthostatic syncope
Orthostatic syncope 		2 0 1 0.33 0 0
CUI: C1868524
Disease: Autonomic erectile dysfunction
Autonomic erectile dysfunction 		2 0 1 0.33 0 0
CUI: C4022830
Disease: Heavy proteinuria
Heavy proteinuria 		2 0 1 0.33 0 0
CUI: C4746986
Disease: ALPORT SYNDROME 1, X-LINKED
ALPORT SYNDROME 1, X-LINKED 		2 0 1 0.33 0 0
CUI: C0012602
Disease: Dirofilariasis
Dirofilariasis 		3 0 1 0.25 0 0
CUI: C0277192
Disease: Infection by Spirocerca
Infection by Spirocerca 		3 0 1 0.25 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 0.25 0 0
CUI: C1518715
Disease: Ovarian Fetiform Teratoma
Ovarian Fetiform Teratoma 		3 0 1 0.25 0 0
CUI: C1835672
Disease: Palmoplantar Keratoderma with Deafness
Palmoplantar Keratoderma with Deafness 		3 0 1 0.25 0 0
CUI: C3151897
Disease: DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL 		3 0 1 0.25 0 0
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		3 0 1 0.25 0 0
CUI: C4274324
Disease: Genetic recurrent myoglobinuria
Genetic recurrent myoglobinuria 		3 0 1 0.25 0 0
CUI: C4023481
Disease: EEG with focal spikes
EEG with focal spikes 		4 0 1 0.20 0 0
CUI: C4531094
Disease: Abnormal mitral valve physiology
Abnormal mitral valve physiology 		4 0 1 0.20 0 0