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: C0398562
Disease: Triose phosphate isomerase deficiency
Triose phosphate isomerase deficiency 		1 0 1 0.50 0 0
CUI: C1858529
Disease: Denervation of the diaphragm
Denervation of the diaphragm 		1 0 1 0.50 0 0
CUI: C1860808
Disease: Triosephosphate Isomerase Deficiency
Triosephosphate Isomerase Deficiency 		1 9 1 0.50 1 8.3E-02
CUI: C3278953
Disease: Axonal polyneuropathy
Axonal polyneuropathy 		1 0 1 0.50 0 0
CUI: C4015349
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S 		1 32 1 0.50 1 2.9E-02
CUI: C4016412
Disease: TRIOSEPHOSPHATE ISOMERASE MANCHESTER
TRIOSEPHOSPHATE ISOMERASE MANCHESTER 		1 0 1 0.50 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 0.33 0 0
CUI: C0752251
Disease: Muscle Disease Manifestations
Muscle Disease Manifestations 		2 0 1 0.33 0 0
CUI: C4505386
Disease: Giardia duodenalis Infection
Giardia duodenalis Infection 		2 0 1 0.33 0 0
CUI: C0751381
Disease: Foley-Denny-Brown Syndrome
Foley-Denny-Brown Syndrome 		3 0 1 0.25 0 0
CUI: C0752252
Disease: Neuromuscular Manifestations
Neuromuscular Manifestations 		3 0 1 0.25 0 0
CUI: C4023471
Disease: EEG with abnormally slow frequencies
EEG with abnormally slow frequencies 		3 0 1 0.25 0 0
CUI: C0085407
Disease: Microsporidiosis
Microsporidiosis 		4 0 1 0.20 0 0
CUI: C3277687
Disease: Central nervous system degeneration
Central nervous system degeneration 		4 0 1 0.20 0 0
CUI: C4025097
Disease: Ventilator dependence with inability to wean
Ventilator dependence with inability to wean 		4 0 1 0.20 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		5 0 1 0.17 0 0
CUI: C3665488
Disease: Familial Osteochondritis Dissecans
Familial Osteochondritis Dissecans 		5 0 1 0.17 0 0
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		13 0 2 0.15 0 0
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga 		7 0 1 0.12 0 0
CUI: C0154681
Disease: Anterior Horn Cell Disease
Anterior Horn Cell Disease 		8 0 1 0.11 0 0
CUI: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		8 0 1 0.11 0 0
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state 		8 0 1 0.11 0 0
CUI: C0235983
Disease: Normochromic anemia
Normochromic anemia 		9 0 1 1.0E-01 0 0
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 1 1.0E-01 0 0
CUI: C0857501
Disease: Acute schizophrenia
Acute schizophrenia 		9 0 1 1.0E-01 0 0