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: C4024929
Disease: Slowed slurred speech
Slowed slurred speech 		5 0 3 0.50 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder 		11 0 4 0.36 0 0
CUI: C4024610
Disease: Leg muscle stiffness
Leg muscle stiffness 		13 0 4 0.31 0 0
CUI: C1142448
Disease: Apraxia of eyelid
Apraxia of eyelid 		5 0 2 0.29 0 0
CUI: C0919678
Disease: Protein S measurement
Protein S measurement 		1 0 1 0.25 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 3 0.25 0 0
CUI: C3809811
Disease: PARKINSON DISEASE 19A, JUVENILE-ONSET
PARKINSON DISEASE 19A, JUVENILE-ONSET 		1 0 1 0.25 0 0
CUI: C3809824
Disease: PARKINSON DISEASE 20, EARLY-ONSET
PARKINSON DISEASE 20, EARLY-ONSET 		1 0 1 0.25 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 0.25 0 0
CUI: C4310802
Disease: PARKINSON DISEASE 19B, EARLY-ONSET
PARKINSON DISEASE 19B, EARLY-ONSET 		1 0 1 0.25 0 0
CUI: C4479313
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53 		1 0 1 0.25 0 0
CUI: C0339652
Disease: Vertical gaze palsy
Vertical gaze palsy 		2 0 1 0.20 0 0
CUI: C3805715
Disease: Short stepped shuffling gait
Short stepped shuffling gait 		16 0 3 0.18 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 1 0.17 0 0
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue 		20 0 3 0.14 0 0
CUI: C0268279
Disease: Lipofuscinosis
Lipofuscinosis 		4 0 1 0.14 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 2 0.14 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 2 0.14 0 0
CUI: C2242579
Disease: Lingual dystonia
Lingual dystonia 		4 0 1 0.14 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 4 0.13 0 0
CUI: C0270871
Disease: Facial Myokymia
Facial Myokymia 		5 0 1 0.12 0 0
CUI: C0887866
Disease: Monckeberg Medial Calcific Sclerosis
Monckeberg Medial Calcific Sclerosis 		5 0 1 0.12 0 0
CUI: C1834207
Disease: Ceroid Lipofuscinosis, Neuronal, Parry Type
Ceroid Lipofuscinosis, Neuronal, Parry Type 		5 0 1 0.12 0 0
CUI: C2919166
Disease: Autosomal dominant focal segmental glomerulosclerosis
Autosomal dominant focal segmental glomerulosclerosis 		5 0 1 0.12 0 0
CUI: C0852950
Disease: Atherosclerosis obliterans
Atherosclerosis obliterans 		6 0 1 0.11 0 0