Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Classical Lissencephalies and Subcortical Band Heterotopias
2 0 2 0.67 0 0
CUI: C2931857
Disease: Double cortex
Double cortex
4 0 2 0.40 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia
1 0 1 0.33 0 0
Lissencephaly and agenesis of corpus callosum
1 11 1 0.33 9 0.28
CUI: C4284594
Disease: BAND HETEROTOPIA
BAND HETEROTOPIA
5 0 2 0.33 0 0
Chromosome 17p13.3 Duplication Syndrome
2 0 1 0.25 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly
14 0 3 0.21 0 0
CUI: C0008519
Disease: Ectopic Tissue
Ectopic Tissue
3 0 1 0.20 0 0
CUI: C0016788
Disease: Fucosidase Deficiency Disease
Fucosidase Deficiency Disease
3 0 1 0.20 0 0
Lissencephaly with cerebellar hypoplasia
4 0 1 0.17 0 0
CUI: C0751246
Disease: Illusions, Visual
Illusions, Visual
5 0 1 0.14 0 0
CUI: C1853618
Disease: Perivascular spaces
Perivascular spaces
5 0 1 0.14 0 0
CUI: C1838702
Disease: Retinitis Pigmentosa 13
Retinitis Pigmentosa 13
6 0 1 0.12 0 0
CUI: C4025884
Disease: Abnormality of upper lip
Abnormality of upper lip
6 0 1 0.12 0 0
CUI: C0431375
Disease: Classical Lissencephaly
Classical Lissencephaly
25 0 3 0.12 0 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait
7 0 1 0.11 0 0
CUI: C0281328
Disease: Adult Subependymoma
Adult Subependymoma
7 0 1 0.11 0 0
CUI: C0742078
Disease: Mass lesion of brain
Mass lesion of brain
7 0 1 0.11 0 0
CUI: C0393699
Disease: Symptomatic Infantile Spasms
Symptomatic Infantile Spasms
8 0 1 1.0E-01 0 0
CUI: C0406191
Disease: Pseudofolliculitis
Pseudofolliculitis
8 0 1 1.0E-01 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia
30 0 3 1.0E-01 0 0
CUI: C1879312
Disease: Agyria
Agyria
20 0 2 9.5E-02 0 0
CUI: C0156221
Disease: Acute glomerulonephritis
Acute glomerulonephritis
9 0 1 9.1E-02 0 0
SUBCORTICAL BAND HETEROTOPIA, X-LINKED
10 0 1 8.3E-02 0 0
CUI: C0206725
Disease: Subependymal Glioma
Subependymal Glioma
13 0 1 6.7E-02 0 0