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: C2220255
Disease: Motor disturbances
Motor disturbances
16 0 6 0.12 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy
8 0 5 0.12 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease
9 0 4 9.3E-02 0 0
Primary Progressive Nonfluent Aphasia
21 0 5 9.3E-02 0 0
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis
33 0 6 9.2E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure
12 0 4 8.7E-02 0 0
Neonatal Hypoxic Ischemic Encephalopathy
26 0 5 8.5E-02 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction
16 0 4 8.0E-02 0 0
CUI: C0262424
Disease: CNS DEGENERATION
CNS DEGENERATION
4 0 3 7.7E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 4 7.7E-02 0 0
CUI: C0270952
Disease: Muscular Dystrophy, Oculopharyngeal
Muscular Dystrophy, Oculopharyngeal
33 0 5 7.6E-02 0 0
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial
19 0 4 7.5E-02 0 0
Left anterior descending coronary artery occlusion
5 0 3 7.5E-02 0 0
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology
20 0 4 7.4E-02 0 0
CUI: C0270985
Disease: Alcohol myopathy
Alcohol myopathy
6 0 3 7.3E-02 0 0
Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive
6 0 3 7.3E-02 0 0
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5
6 0 3 7.3E-02 0 0
CUI: C0018425
Disease: Gyrate Atrophy
Gyrate Atrophy
8 0 3 7.0E-02 0 0
CUI: C0476237
Disease: Metabolic symptoms
Metabolic symptoms
9 0 3 6.8E-02 0 0
CUI: C0546483
Disease: Lung cyst
Lung cyst
9 0 3 6.8E-02 0 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression
9 0 3 6.8E-02 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy
9 0 3 6.8E-02 0 0
CUI: C0267375
Disease: Chronic colitis
Chronic colitis
57 0 6 6.7E-02 0 0
CUI: C0546983
Disease: Post-Concussion Syndrome
Post-Concussion Syndrome
11 0 3 6.5E-02 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 5 6.5E-02 0 0