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: C0750968
Disease: Central Nervous System Metabolic Disorders
Central Nervous System Metabolic Disorders 		2 0 1 7.1E-02 0 0
CUI: C0751743
Disease: Metabolic Disorder, Central Nervous System, Acquired
Metabolic Disorder, Central Nervous System, Acquired 		2 0 1 7.1E-02 0 0
CUI: C0751744
Disease: Brain Diseases, Metabolic, Acquired
Brain Diseases, Metabolic, Acquired 		2 0 1 7.1E-02 0 0
CUI: C0795818
Disease: Chromosome 7 ring syndrome
Chromosome 7 ring syndrome 		2 0 1 7.1E-02 0 0
CUI: C0856636
Disease: Transient hemiparesis
Transient hemiparesis 		2 0 1 7.1E-02 0 0
CUI: C1135773
Disease: Acquired Metabolic Diseases, Nervous System
Acquired Metabolic Diseases, Nervous System 		2 0 1 7.1E-02 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 7.1E-02 0 0
CUI: C1275047
Disease: Radiation-induced xerostomia
Radiation-induced xerostomia 		2 0 1 7.1E-02 0 0
CUI: C1735856
Disease: Migraine with Typical Aura
Migraine with Typical Aura 		2 0 1 7.1E-02 0 0
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		2 0 1 7.1E-02 0 0
CUI: C1842704
Disease: GAUCHER DISEASE, PERINATAL LETHAL
GAUCHER DISEASE, PERINATAL LETHAL 		2 18 1 7.1E-02 1 5.6E-02
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 1 7.1E-02 0 0
CUI: C1846367
Disease: Spinocerebellar ataxia 19
Spinocerebellar ataxia 19 		2 0 1 7.1E-02 0 0
CUI: C1865332
Disease: Transient unilateral blurring of vision
Transient unilateral blurring of vision 		2 0 1 7.1E-02 0 0
CUI: C2673635
Disease: Combined Saposin Deficiency
Combined Saposin Deficiency 		2 0 1 7.1E-02 0 0
CUI: C2677843
Disease: Episodic Ataxia, Type 7
Episodic Ataxia, Type 7 		2 0 1 7.1E-02 0 0
CUI: C2939445
Disease: Carcinoma in situ of bronchus
Carcinoma in situ of bronchus 		2 0 1 7.1E-02 0 0
CUI: C3150738
Disease: Antibody Deficiency due to Defect in CD19
Antibody Deficiency due to Defect in CD19 		2 0 1 7.1E-02 0 0
CUI: C3150974
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3 		2 0 1 7.1E-02 0 0
CUI: C3495554
Disease: Homocarnosinase deficiency
Homocarnosinase deficiency 		2 0 1 7.1E-02 0 0
CUI: C3553660
Disease: Malan overgrowth syndrome
Malan overgrowth syndrome 		2 0 1 7.1E-02 0 0
CUI: C3806306
Disease: Periarticular subcutaneous nodules
Periarticular subcutaneous nodules 		2 0 1 7.1E-02 0 0
CUI: C4020790
Disease: Medullary sponge kidney disease
Medullary sponge kidney disease 		2 0 1 7.1E-02 0 0
CUI: C4025031
Disease: Aplasia/hypoplasia of the humerus
Aplasia/hypoplasia of the humerus 		2 0 1 7.1E-02 0 0
CUI: C4025537
Disease: Humerus varus
Humerus varus 		2 0 1 7.1E-02 0 0