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: C4703464
Disease: Abnormal aortic valve physiology
Abnormal aortic valve physiology 		4 0 3 0.60 0 0
CUI: C3275686
Disease: CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY
CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY 		2 0 2 0.50 0 0
CUI: C4751573
Disease: Periodic paralysis with later-onset distal motor neuropathy
Periodic paralysis with later-onset distal motor neuropathy 		2 0 2 0.50 0 0
CUI: C0277355
Disease: Flea Infestation
Flea Infestation 		5 0 2 0.29 0 0
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis 		1 0 1 0.25 0 0
CUI: C0006897
Disease: Capillariasis
Capillariasis 		1 0 1 0.25 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis 		1 0 1 0.25 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness 		1 0 1 0.25 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection 		1 0 1 0.25 0 0
CUI: C1838868
Disease: Corticospinal tract atrophy
Corticospinal tract atrophy 		1 0 1 0.25 0 0
CUI: C1838916
Disease: ATAXIA AND POLYNEUROPATHY, ADULT-ONSET
ATAXIA AND POLYNEUROPATHY, ADULT-ONSET 		1 0 1 0.25 0 0
CUI: C1839022
Disease: Striatonigral Degeneration, Infantile, Mitochondrial
Striatonigral Degeneration, Infantile, Mitochondrial 		1 0 1 0.25 0 0
CUI: C3275684
Disease: MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1 		1 0 1 0.25 0 0
CUI: C4016601
Disease: SIDEROBLASTIC ANEMIA, ACQUIRED IDIOPATHIC
SIDEROBLASTIC ANEMIA, ACQUIRED IDIOPATHIC 		1 0 1 0.25 0 0
CUI: C4016602
Disease: CYTOCHROME c OXIDASE I DEFICIENCY
CYTOCHROME c OXIDASE I DEFICIENCY 		1 0 1 0.25 0 0
CUI: C4016603
Disease: SEIZURES AND LACTIC ACIDOSIS
SEIZURES AND LACTIC ACIDOSIS 		1 0 1 0.25 0 0
CUI: C4225415
Disease: MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3
MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3 		1 0 1 0.25 0 0
CUI: C4755299
Disease: MT-ATP6-related mitochondrial spastic paraplegia
MT-ATP6-related mitochondrial spastic paraplegia 		1 0 1 0.25 0 0
CUI: C1328349
Disease: Neuropathy ataxia and retinis pigmentosa
Neuropathy ataxia and retinis pigmentosa 		7 0 2 0.22 0 0
CUI: C0009225
Disease: Coenuriasis
Coenuriasis 		2 0 1 0.20 0 0
CUI: C0036231
Disease: Sarcocystosis
Sarcocystosis 		2 0 1 0.20 0 0
CUI: C0086227
Disease: Enterobiasis
Enterobiasis 		2 0 1 0.20 0 0
CUI: C0856716
Disease: Asthma aspirin-sensitive
Asthma aspirin-sensitive 		8 0 2 0.20 0 0
CUI: C1838877
Disease: Myoglobinuria, Recurrent
Myoglobinuria, Recurrent 		2 0 1 0.20 0 0
CUI: C4757950
Disease: Isolated ATP synthase deficiency
Isolated ATP synthase deficiency 		8 0 2 0.20 0 0