Source: CURATED ×
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: C0231687
Disease: Spastic gait
Spastic gait 		4 0 4 1.00 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		4 2 4 1.00 1 0.11
CUI: C0231689
Disease: Gait, Athetotic
Gait, Athetotic 		4 0 4 1.00 0 0
CUI: C0231693
Disease: Charcot Gait
Charcot Gait 		4 0 4 1.00 0 0
CUI: C0231694
Disease: Gait, Festinating
Gait, Festinating 		4 0 4 1.00 0 0
CUI: C0231695
Disease: Cerebellar ataxic gait
Cerebellar ataxic gait 		4 0 4 1.00 0 0
CUI: C0231696
Disease: Gait, Hemiplegic
Gait, Hemiplegic 		4 0 4 1.00 0 0
CUI: C0231698
Disease: Gait, Scissors
Gait, Scissors 		4 0 4 1.00 0 0
CUI: C0234996
Disease: Gait, Rigid
Gait, Rigid 		4 0 4 1.00 0 0
CUI: C0235000
Disease: Gait, Broadened
Gait, Broadened 		4 0 4 1.00 0 0
CUI: C0337210
Disease: Gait, Stumbling
Gait, Stumbling 		4 0 4 1.00 0 0
CUI: C0427128
Disease: Rapid Fatigue of Gait
Rapid Fatigue of Gait 		4 0 4 1.00 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		4 0 4 1.00 0 0
CUI: C0427169
Disease: Marche a Petit Pas
Marche a Petit Pas 		4 0 4 1.00 0 0
CUI: C0427177
Disease: Gait, Hysterical
Gait, Hysterical 		4 0 4 1.00 0 0
CUI: C0751829
Disease: Gait Disorder, Sensorimotor
Gait Disorder, Sensorimotor 		4 0 4 1.00 0 0
CUI: C0751830
Disease: Gait Disorders, Neurologic
Gait Disorders, Neurologic 		4 0 4 1.00 0 0
CUI: C0751831
Disease: Gait, Frontal
Gait, Frontal 		4 0 4 1.00 0 0
CUI: C0751832
Disease: Gait, Widebased
Gait, Widebased 		4 0 4 1.00 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		5 0 4 0.80 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		1 0 1 0.25 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		1 0 1 0.25 0 0
CUI: C1839909
Disease: CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED
CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED 		1 0 1 0.25 0 0
CUI: C3554605
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 		1 0 1 0.25 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		2 0 1 0.20 0 0