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: C0020039
Disease: Hostility
Hostility 		1 0 1 1.4E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention 		1 0 1 1.4E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 1.4E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal 		1 0 1 1.4E-02 0 0
CUI: C0155002
Disease: Sudden visual loss
Sudden visual loss 		1 0 1 1.4E-02 0 0
CUI: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 1.4E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 1.4E-02 0 0
CUI: C0264558
Disease: Tension Pneumothorax
Tension Pneumothorax 		1 0 1 1.4E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 1.4E-02 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 1.4E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 1.4E-02 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 1.4E-02 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 1.4E-02 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 1.4E-02 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 1.4E-02 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 1.4E-02 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 1.4E-02 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 1.4E-02 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 1.4E-02 0 0
CUI: C0877306
Disease: Iris hyperpigmentation
Iris hyperpigmentation 		1 0 1 1.4E-02 0 0
CUI: C1275836
Disease: D - transposition of the great vessels
D - transposition of the great vessels 		1 0 1 1.4E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 1.4E-02 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 1.4E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 1.4E-02 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 1.4E-02 0 0