Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Behavioral variant of frontotemporal dementia
35 0 6 0.12 0 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
8 0 3 0.12 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia
56 0 8 0.12 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 8 0.12 0 0
CUI: C0026884
Disease: Mutism
Mutism
47 0 7 0.12 0 0
Urinary bladder sphincter dysfunction
28 0 5 0.12 0 0
CUI: C0919974
Disease: Abulia
Abulia
9 0 3 0.12 0 0
CUI: C0522224
Disease: Paralysed
Paralysed
68 0 9 0.11 0 0
CUI: C0030360
Disease: Papillon-Lefevre Disease
Papillon-Lefevre Disease
29 0 5 0.11 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic
30 0 5 0.11 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality
10 0 3 0.11 0 0
Fatigable weakness of respiratory muscles
60 0 8 0.11 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity
10 0 3 0.11 0 0
CUI: C0742038
Disease: Cerebellar signs
Cerebellar signs
24 0 4 1.0E-01 0 0
CUI: C1853396
Disease: Primary lateral sclerosis juvenile
Primary lateral sclerosis juvenile
2 0 2 1.0E-01 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior
13 0 3 1.0E-01 0 0
Amyotrophic Lateral Sclerosis, Guam Form
36 0 5 9.8E-02 0 0
CUI: C0424290
Disease: Compulsive hoarding
Compulsive hoarding
14 0 3 9.7E-02 0 0
CUI: C4021584
Disease: Frontotemporal cerebral atrophy
Frontotemporal cerebral atrophy
14 0 3 9.7E-02 0 0
CUI: C0003635
Disease: Apraxias
Apraxias
71 0 8 9.6E-02 0 0
Dermatopathia pigmentosa reticularis
3 0 2 9.5E-02 0 0
Polyglucosan Body Disease, Adult Form
3 0 2 9.5E-02 0 0
CUI: C1853723
Disease: MYOPATHY, DISTAL 2
MYOPATHY, DISTAL 2
3 0 2 9.5E-02 0 0
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY
3 0 2 9.5E-02 0 0
Impaired vibration sensation in the lower limbs
39 0 5 9.3E-02 0 0