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 9.1E-02 0 0
CUI: C0021712
Disease: Myoclonus, Intention
Myoclonus, Intention
1 0 1 9.1E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing
1 0 1 9.1E-02 0 0
CUI: C0030214
Disease: Myoclonus, Palatal
Myoclonus, Palatal
1 0 1 9.1E-02 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia
1 0 1 9.1E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia
1 0 1 9.1E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing
1 0 1 9.1E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia
1 0 1 9.1E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing
1 0 1 9.1E-02 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal
1 0 1 9.1E-02 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex
1 0 1 9.1E-02 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity
1 0 1 9.1E-02 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental
1 0 1 9.1E-02 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal
1 0 1 9.1E-02 0 0
CUI: C0751353
Disease: Myoclonus, Upper Extremity
Myoclonus, Upper Extremity
1 0 1 9.1E-02 0 0
CUI: C0859389
Disease: DDS syndrome
DDS syndrome
1 0 1 9.1E-02 0 0
D - transposition of the great vessels
1 0 1 9.1E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia
1 0 1 9.1E-02 0 0
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
1 0 1 9.1E-02 0 0
Rett Syndrome, Preserved Speech Variant
1 0 1 9.1E-02 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation
1 0 1 9.1E-02 0 0
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
1 0 1 9.1E-02 0 0
Mental Retardation, X-Linked, Syndromic 13
1 0 1 9.1E-02 0 0
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79
1 0 1 9.1E-02 0 0
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
1 0 1 9.1E-02 0 0