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: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood
8 0 4 0.14 0 0
CUI: C0233488
Disease: Feeling despair
Feeling despair
21 0 4 9.5E-02 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
10 0 3 9.4E-02 0 0
CUI: C0040820
Disease: Trematode Infections
Trematode Infections
12 0 3 8.8E-02 0 0
CUI: C0751434
Disease: Classical phenylketonuria
Classical phenylketonuria
42 0 5 8.1E-02 0 0
CUI: C0751435
Disease: Hyperphenylalaninaemia
Hyperphenylalaninaemia
30 0 4 7.8E-02 0 0
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis
18 0 3 7.5E-02 0 0
CUI: C0748073
Disease: psychosocial stressor
psychosocial stressor
18 0 3 7.5E-02 0 0
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis
19 0 3 7.3E-02 0 0
CUI: C0278110
Disease: Hemiplegia, Crossed
Hemiplegia, Crossed
5 0 2 7.1E-02 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
6 0 2 6.9E-02 0 0
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2
6 0 2 6.9E-02 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma
22 0 3 6.8E-02 0 0
CUI: C3890602
Disease: Bodily Pain
Bodily Pain
22 0 3 6.8E-02 0 0
CUI: C0030508
Disease: Parasomnia
Parasomnia
7 0 2 6.7E-02 0 0
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual
39 5 4 6.7E-02 1 0.17
CUI: C0395920
Disease: Migrainous vertigo
Migrainous vertigo
7 0 2 6.7E-02 0 0
CUI: C0751771
Disease: Sleep Bruxism
Sleep Bruxism
7 4 2 6.7E-02 1 0.20
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
7 0 2 6.7E-02 0 0
CUI: C1963933
Disease: Punding
Punding
7 0 2 6.7E-02 0 0
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
24 0 3 6.5E-02 0 0
CUI: C0018991
Disease: Hemiplegia
Hemiplegia
41 0 4 6.5E-02 0 0
CUI: C0013423
Disease: Dystonia Musculorum Deformans
Dystonia Musculorum Deformans
26 0 3 6.2E-02 0 0
CUI: C0028850
Disease: Ocular Motility Disorders
Ocular Motility Disorders
9 0 2 6.2E-02 0 0
CUI: C0393598
Disease: Idiopathic familial dystonia
Idiopathic familial dystonia
9 0 2 6.2E-02 0 0