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: C3151343
Disease: SPINOCEREBELLAR ATAXIA 32
SPINOCEREBELLAR ATAXIA 32
2 0 1 0.20 0 0
CUI: C3715156
Disease: AMYOTROPHIC LATERAL SCLEROSIS 20
AMYOTROPHIC LATERAL SCLEROSIS 20
2 0 1 0.20 0 0
CUI: C3899369
Disease: Direct Extension
Direct Extension
2 0 1 0.20 0 0
CUI: C0032586
Disease: Polyradiculopathy
Polyradiculopathy
3 0 1 0.17 0 0
CUI: C0233754
Disease: Derealization
Derealization
3 0 1 0.17 0 0
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency
3 0 1 0.17 0 0
CUI: C1260874
Disease: Infective dermatitis
Infective dermatitis
3 0 1 0.17 0 0
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
3 0 1 0.17 0 0
CUI: C2363813
Disease: Short-term memory impairment
Short-term memory impairment
3 0 1 0.17 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis
12 0 2 0.14 0 0
CUI: C0221165
Disease: Diplegia
Diplegia
4 0 1 0.14 0 0
CUI: C0231689
Disease: Gait, Athetotic
Gait, Athetotic
4 0 1 0.14 0 0
CUI: C0231693
Disease: Charcot Gait
Charcot Gait
4 0 1 0.14 0 0
CUI: C0231694
Disease: Gait, Festinating
Gait, Festinating
4 0 1 0.14 0 0
CUI: C0231695
Disease: Cerebellar ataxic gait
Cerebellar ataxic gait
4 0 1 0.14 0 0
CUI: C0231696
Disease: Gait, Hemiplegic
Gait, Hemiplegic
4 0 1 0.14 0 0
CUI: C0234996
Disease: Gait, Rigid
Gait, Rigid
4 0 1 0.14 0 0
CUI: C0235000
Disease: Gait, Broadened
Gait, Broadened
4 0 1 0.14 0 0
CUI: C0337210
Disease: Gait, Stumbling
Gait, Stumbling
4 0 1 0.14 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia
4 0 1 0.14 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure
12 0 2 0.14 0 0
CUI: C0427128
Disease: Rapid Fatigue of Gait
Rapid Fatigue of Gait
4 0 1 0.14 0 0
CUI: C0427169
Disease: Marche a Petit Pas
Marche a Petit Pas
4 0 1 0.14 0 0
CUI: C0427177
Disease: Gait, Hysterical
Gait, Hysterical
4 0 1 0.14 0 0
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis
4 0 1 0.14 0 0