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: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 0.11 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 0.11 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 0.11 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 0.11 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 0.11 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity 		1 0 1 0.11 0 0
CUI: C0751668
Disease: Machado-Joseph Disease Type I
Machado-Joseph Disease Type I 		1 0 1 0.11 0 0
CUI: C0751669
Disease: Machado-Joseph Disease Type II
Machado-Joseph Disease Type II 		1 0 1 0.11 0 0
CUI: C0751670
Disease: Machado-Joseph Disease Type III
Machado-Joseph Disease Type III 		1 0 1 0.11 0 0
CUI: C0751671
Disease: Machado-Joseph Disease Type IV
Machado-Joseph Disease Type IV 		1 0 1 0.11 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 0.11 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.11 0 0
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 0.11 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 0.11 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 8 1 0.11 1 0.11
CUI: C1859231
Disease: Hypoplastic olfactory lobes
Hypoplastic olfactory lobes 		1 0 1 0.11 0 0
CUI: C1862359
Disease: Facial-lingual fasciculations
Facial-lingual fasciculations 		1 0 1 0.11 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 27 1 0.11 1 3.6E-02
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 0.11 0 0
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		1 43 1 0.11 1 2.3E-02
CUI: C2053440
Disease: Thin lower lip vermilion
Thin lower lip vermilion 		1 0 1 0.11 0 0
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 0 1 0.11 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.11 0 0
CUI: C2750720
Disease: Cone-Rod Dystrophy 13
Cone-Rod Dystrophy 13 		1 0 1 0.11 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 0.11 0 0