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: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity
1 0 1 3.7E-02 0 0
Pleural Epithelioid Hemangioendothelioma
1 0 1 3.7E-02 0 0
Congenital vertical talus, bilateral
1 0 1 3.7E-02 0 0
Multiple system atrophy, cerebellar variant
1 0 1 3.7E-02 0 0
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
1 0 1 3.7E-02 0 0
Amyotrophic lateral sclerosis, type 6
1 0 1 3.7E-02 0 0
CUI: C3150677
Disease: AUTISM, SUSCEPTIBILITY TO, 16
AUTISM, SUSCEPTIBILITY TO, 16
1 0 1 3.7E-02 0 0
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
TREMOR, HEREDITARY ESSENTIAL, 4
1 4 1 3.7E-02 2 2.9E-02
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement
1 0 1 3.7E-02 0 0
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
1 0 1 3.7E-02 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19
1 0 1 3.7E-02 0 0
Spindle Cell/Sclerosing Rhabdomyosarcoma
1 0 1 3.7E-02 0 0
Deep cerebral white matter hyperdensities
1 0 1 3.7E-02 0 0
Epileptic encephalopathy with global cerebral demyelination
1 0 1 3.7E-02 0 0
Metastatic Oral Cavity Squamous Cell Carcinoma
1 0 1 3.7E-02 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0
87 0 4 3.6E-02 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0
87 0 4 3.6E-02 0 0
CUI: C0221166
Disease: Paraparesis
Paraparesis
31 0 2 3.6E-02 0 0
CUI: C0239842
Disease: Tremor of hands
Tremor of hands
31 0 2 3.6E-02 0 0
Lower Extremity Deformities, Congenital
2 0 1 3.6E-02 0 0
CUI: C0561843
Disease: Memory, Episodic
Memory, Episodic
2 0 1 3.6E-02 0 0
CUI: C0581321
Disease: Vertebral osteoporosis
Vertebral osteoporosis
2 0 1 3.6E-02 0 0
CUI: C0796059
Disease: Oculopalatoskeletal syndrome
Oculopalatoskeletal syndrome
2 0 1 3.6E-02 0 0
CUI: C1290871
Disease: Disorder of hand
Disorder of hand
2 0 1 3.6E-02 0 0
CUI: C1335512
Disease: Prostate Lymphoma
Prostate Lymphoma
2 0 1 3.6E-02 0 0