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: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis
61 0 14 0.13 0 0
CUI: C0424448
Disease: Mask-like facies
Mask-like facies
64 0 14 0.13 0 0
CUI: C0262361
Disease: Growth abnormality
Growth abnormality
49 0 12 0.13 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 20 0.13 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment
86 0 16 0.12 0 0
CUI: C1856507
Disease: Bulbar signs
Bulbar signs
33 0 10 0.12 0 0
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
103 0 17 0.12 0 0
Decreased number of peripheral myelinated nerve fibers
28 0 9 0.12 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
86 0 15 0.12 0 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction
87 0 15 0.12 0 0
Aplasia/Hypoplasia of the cerebellum
116 0 18 0.12 0 0
Sensorineural hearing loss, bilateral
117 0 18 0.11 0 0
CUI: C4553765
Disease: Memory Impairment, CTCAE 5.0
Memory Impairment, CTCAE 5.0
108 0 17 0.11 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 17 0.11 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
80 0 14 0.11 0 0
CUI: C0376480
Disease: Gingival Overgrowth
Gingival Overgrowth
100 0 16 0.11 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 37 0.11 0 0
CUI: C0271196
Disease: Scotoma, Centrocecal
Scotoma, Centrocecal
12 0 7 0.11 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment
84 0 14 0.11 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 16 0.10 0 0
CUI: C0878575
Disease: Peripheral demyelination
Peripheral demyelination
27 3 8 0.10 1 0.14
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 14 0.10 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism
92 0 14 0.10 0 0
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism
93 0 14 0.10 0 0
CUI: C0152020
Disease: Gastroparesis
Gastroparesis
95 0 14 0.10 0 0