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: C0036305
Disease: Schamberg Disease
Schamberg Disease 		6 0 1 0.12 0 0
CUI: C0240231
Disease: Fractures of the long bones
Fractures of the long bones 		6 0 1 0.12 0 0
CUI: C0003079
Disease: Anisocoria
Anisocoria 		7 0 1 0.11 0 0
CUI: C0442833
Disease: Arteriolar hyalinosis
Arteriolar hyalinosis 		7 0 1 0.11 0 0
CUI: C0919645
Disease: Tumour ulceration
Tumour ulceration 		7 0 1 0.11 0 0
CUI: C1855472
Disease: Acute lymphoblastic leukemia with lymphomatous features
Acute lymphoblastic leukemia with lymphomatous features 		7 0 1 0.11 0 0
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		7 0 1 0.11 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 0.11 0 0
CUI: C0154971
Disease: Presenile cataract
Presenile cataract 		8 0 1 1.0E-01 0 0
CUI: C1335377
Disease: periampullary adenocarcinoma
periampullary adenocarcinoma 		8 0 1 1.0E-01 0 0
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 1 1.0E-01 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury 		8 0 1 1.0E-01 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration 		8 0 1 1.0E-01 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 1 9.1E-02 0 0
CUI: C1836527
Disease: Distal sensory impairment of all modalities
Distal sensory impairment of all modalities 		9 0 1 9.1E-02 0 0
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		9 0 1 9.1E-02 0 0
CUI: C4025799
Disease: Ulnar claw
Ulnar claw 		9 0 1 9.1E-02 0 0
CUI: C0334513
Disease: Sarcomatoid Mesothelioma
Sarcomatoid Mesothelioma 		10 0 1 8.3E-02 0 0
CUI: C0949855
Disease: Electron Transport Chain Deficiencies, Mitochondrial
Electron Transport Chain Deficiencies, Mitochondrial 		10 0 1 8.3E-02 0 0
CUI: C1509147
Disease: Histiocytoma
Histiocytoma 		10 0 1 8.3E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 8.3E-02 0 0
CUI: C3697716
Disease: Acute flaccid paralysis
Acute flaccid paralysis 		10 0 1 8.3E-02 0 0
CUI: C4331269
Disease: Sacral Chordoma
Sacral Chordoma 		10 0 1 8.3E-02 0 0
CUI: C1850415
Disease: Microvesicular hepatic steatosis
Microvesicular hepatic steatosis 		11 0 1 7.7E-02 0 0
CUI: C0027902
Disease: Neuropsychological Tests
Neuropsychological Tests 		12 0 1 7.1E-02 0 0