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: C0029438
Disease: Massive Osteolyses
Massive Osteolyses
44 0 1 2.3E-02 0 0
Generalized glycogen storage disease of infants
51 0 1 2.0E-02 0 0
CUI: C0014867
Disease: Esophageal Varices
Esophageal Varices
56 0 1 1.8E-02 0 0
Gerstmann-Straussler-Scheinker Disease
56 0 1 1.8E-02 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease
63 0 1 1.6E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
63 0 1 1.6E-02 0 0
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency
65 0 1 1.5E-02 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
70 0 1 1.4E-02 0 0
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis
72 0 1 1.4E-02 0 0
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
82 0 1 1.2E-02 0 0
CUI: C1857108
Disease: Limitation of joint mobility
Limitation of joint mobility
84 0 1 1.2E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 1 1.2E-02 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 1 1.1E-02 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis
92 0 1 1.1E-02 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy
94 0 1 1.1E-02 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 1 8.6E-03 0 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
121 0 1 8.3E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 1 8.3E-03 0 0
CUI: C0013604
Disease: Edema
Edema
126 0 1 7.9E-03 0 0
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly
127 0 1 7.9E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 7.7E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
144 0 1 6.9E-03 0 0
CUI: C0037299
Disease: Skin Ulcer
Skin Ulcer
151 0 1 6.6E-03 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence
151 0 1 6.6E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign
155 0 1 6.5E-03 0 0