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: C0030552
Disease: Paresis
Paresis
216 49 208 0.38 46 0.51
CUI: C0026848
Disease: Myopathy
Myopathy
634 166 211 0.22 17 7.2E-02
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 16 94 0.15 6 6.2E-02
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
20 19 9 1.6E-02 6 6.0E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 57 163 0.17 8 5.9E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
389 50 122 0.15 7 5.4E-02
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 24 22 3.9E-02 5 4.7E-02
CUI: C0013404
Disease: Dyspnea
Dyspnea
222 26 61 8.8E-02 5 4.6E-02
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 30 84 0.12 5 4.5E-02
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect
61 8 16 2.8E-02 4 4.4E-02
CUI: C3808046
Disease: Breathing dysregulation
Breathing dysregulation
12 8 4 7.4E-03 4 4.4E-02
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass
65 12 19 3.3E-02 4 4.2E-02
CUI: C0040264
Disease: Tinnitus
Tinnitus
103 14 19 3.1E-02 4 4.1E-02
CUI: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow
73 14 27 4.6E-02 4 4.1E-02
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure
319 23 98 0.13 4 3.8E-02
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 62 90 9.8E-02 5 3.5E-02
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy
9 4 8 1.5E-02 3 3.4E-02
CUI: C0030196
Disease: Pain in limb
Pain in limb
16 5 5 9.1E-03 3 3.4E-02
CUI: C0220621
Disease: Childhood Acute Myeloid Leukemia
Childhood Acute Myeloid Leukemia
215 6 20 2.7E-02 3 3.3E-02
CUI: C0038450
Disease: Stridor
Stridor
31 7 14 2.5E-02 3 3.3E-02
CUI: C1865304
Disease: Overfolding of the superior helices
Overfolding of the superior helices
10 7 2 3.7E-03 3 3.3E-02
CUI: C0030554
Disease: Paresthesia
Paresthesia
121 8 45 7.4E-02 3 3.3E-02
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense
33 8 10 1.8E-02 3 3.3E-02
CUI: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex
11 8 7 1.3E-02 3 3.3E-02
CUI: C0037763
Disease: Spasm
Spasm
172 9 61 9.4E-02 3 3.2E-02