Source: ALL
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: C3266164
Disease: Dropped head syndrome
Dropped head syndrome 		0 1 0 0 1 1.5E-02
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity 		1 0 1 3.7E-02 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 3.7E-02 0 0
CUI: C1860446
Disease: Congenital vertical talus, bilateral
Congenital vertical talus, bilateral 		1 0 1 3.7E-02 0 0
CUI: C2732311
Disease: Multiple system atrophy, cerebellar variant
Multiple system atrophy, cerebellar variant 		1 0 1 3.7E-02 0 0
CUI: C2750729
Disease: Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive 		1 0 1 3.7E-02 0 0
CUI: C2931786
Disease: Amyotrophic lateral sclerosis, type 6
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
CUI: C3553661
Disease: CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
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
CUI: C4053999
Disease: Spindle Cell/Sclerosing Rhabdomyosarcoma
Spindle Cell/Sclerosing Rhabdomyosarcoma 		1 0 1 3.7E-02 0 0
CUI: C4293685
Disease: Deep cerebral white matter hyperdensities
Deep cerebral white matter hyperdensities 		1 0 1 3.7E-02 0 0
CUI: C4512050
Disease: Epileptic encephalopathy with global cerebral demyelination
Epileptic encephalopathy with global cerebral demyelination 		1 0 1 3.7E-02 0 0
CUI: C4727684
Disease: Metastatic Oral Cavity Squamous Cell Carcinoma
Metastatic Oral Cavity Squamous Cell Carcinoma 		1 0 1 3.7E-02 0 0
CUI: C0431943
Disease: Lower Extremity Deformities, Congenital
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
CUI: C1708749
Disease: Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes
Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes 		2 0 1 3.6E-02 0 0
CUI: C1850336
Disease: Single interphalangeal crease of fifth finger
Single interphalangeal crease of fifth finger 		2 0 1 3.6E-02 0 0
CUI: C2675186
Disease: LEBER CONGENITAL AMAUROSIS 13
LEBER CONGENITAL AMAUROSIS 13 		2 0 1 3.6E-02 0 0