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: C1879312
Disease: Agyria
Agyria
20 0 7 0.18 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly
14 0 5 0.15 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia
30 3 6 0.12 3 3.1E-02
CUI: C4551968
Disease: Lissencephaly, X-Linked, 1
Lissencephaly, X-Linked, 1
3 0 3 0.12 0 0
CUI: C0266463
Disease: Lissencephaly
Lissencephaly
71 0 10 0.12 0 0
Lissencephaly with cerebellar hypoplasia
4 0 3 0.12 0 0
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly
15 0 4 0.11 0 0
Classical Lissencephalies and Subcortical Band Heterotopias
2 0 2 8.0E-02 0 0
Malformations of Cortical Development
60 0 6 7.6E-02 0 0
CUI: C2931857
Disease: Double cortex
Double cortex
4 0 2 7.4E-02 0 0
CUI: C4284594
Disease: BAND HETEROTOPIA
BAND HETEROTOPIA
5 0 2 7.1E-02 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 5 6.7E-02 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly
40 0 4 6.6E-02 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 9 6.2E-02 0 0
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain
103 0 7 5.8E-02 0 0
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome
14 0 2 5.4E-02 0 0
CUI: C1273957
Disease: Upper limb spasticity
Upper limb spasticity
14 0 2 5.4E-02 0 0
CUI: C0028860
Disease: Oculocerebrorenal Syndrome
Oculocerebrorenal Syndrome
54 0 4 5.3E-02 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 2 5.0E-02 0 0
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis
19 0 2 4.8E-02 0 0
CUI: C0394006
Disease: Dysequilibrium syndrome
Dysequilibrium syndrome
20 0 2 4.7E-02 0 0
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders
20 0 2 4.7E-02 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity
43 0 3 4.6E-02 0 0
CUI: C1868720
Disease: Periventricular Nodular Heterotopia
Periventricular Nodular Heterotopia
45 0 3 4.5E-02 0 0
CUI: C1321905
Disease: Minimal Brain Dysfunction
Minimal Brain Dysfunction
22 0 2 4.4E-02 0 0