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: C4310757
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 2F
PONTOCEREBELLAR HYPOPLASIA, TYPE 2F
1 0 1 1.00 0 0
CUI: C2932714
Disease: Pontocerebellar Hypoplasia Type 2
Pontocerebellar Hypoplasia Type 2
6 0 1 0.17 0 0
CUI: C1261175
Disease: Pontoneocerebellar hypoplasia
Pontoneocerebellar hypoplasia
27 0 1 3.7E-02 0 0
Congenital pontocerebellar hypoplasia
32 0 1 3.1E-02 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly
39 0 1 2.6E-02 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly
67 0 1 1.5E-02 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
160 0 1 6.3E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 4.0E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 4.0E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 3.1E-03 0 0
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
378 0 1 2.6E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking
391 0 1 2.6E-03 0 0
High density lipoprotein measurement
545 0 1 1.8E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 1 1.7E-03 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
656 0 1 1.5E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 1 1.0E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy
1215 0 1 8.2E-04 0 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
1825 0 1 5.5E-04 0 0
CUI: C0005890
Disease: Body Height
Body Height
1903 0 1 5.3E-04 0 0
CUI: C0036572
Disease: Seizures
Seizures
2152 0 1 4.6E-04 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
2165 0 1 4.6E-04 0 0