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: C0751037
Disease: Cockayne Syndrome, Type III
Cockayne Syndrome, Type III
2 0 2 0.33 0 0
Patchy demyelination of subcortical white matter
2 0 2 0.33 0 0
Ivory epiphyses of the phalanges of the hand
3 0 2 0.29 0 0
CUI: C1849953
Disease: Square pelvis bone
Square pelvis bone
4 0 2 0.25 0 0
CUI: C1857645
Disease: Slender nose
Slender nose
4 0 2 0.25 0 0
Increased cellular sensitivity to UV light
4 0 2 0.25 0 0
CUI: C4025610
Disease: Peripheral dysmyelination
Peripheral dysmyelination
4 0 2 0.25 0 0
CUI: C1837767
Disease: Loss of facial adipose tissue
Loss of facial adipose tissue
6 0 2 0.20 0 0
CUI: C0234174
Disease: Sucking reflex
Sucking reflex
1 0 1 0.17 0 0
CUI: C0234966
Disease: Astasia
Astasia
1 0 1 0.17 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome
1 0 1 0.17 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis
1 0 1 0.17 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration
1 0 1 0.17 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect
1 0 1 0.17 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait
1 0 1 0.17 0 0
CUI: C1335911
Disease: Salivary Gland Sialoblastoma
Salivary Gland Sialoblastoma
1 0 1 0.17 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia
1 0 1 0.17 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex
1 0 1 0.17 0 0
Supranuclear Palsy, Progressive, 1, Atypical
1 0 1 0.17 0 0
Subcortical white matter calcifications
1 0 1 0.17 0 0
CUI: C1851431
Disease: Cerebellar calcifications
Cerebellar calcifications
1 0 1 0.17 0 0
CUI: C1857652
Disease: Thymic hormone decreased
Thymic hormone decreased
1 0 1 0.17 0 0
Second metatarsal posteriorly placed
1 0 1 0.17 0 0
CUI: C1861799
Disease: Catatrichy
Catatrichy
1 0 1 0.17 0 0
Yemenite deaf-blind hypopigmentation syndrome
1 0 1 0.17 0 0