Source: ALL
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: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 5.0E-02 0 0
CUI: C1837229
Disease: Muscular Dystrophy, Congenital, Type 1D
Muscular Dystrophy, Congenital, Type 1D 		1 0 1 5.0E-02 0 0
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		1 0 1 5.0E-02 0 0
CUI: C1850871
Disease: Hypoplasia of the pyramidal tract
Hypoplasia of the pyramidal tract 		1 0 1 5.0E-02 0 0
CUI: C1857977
Disease: MICROHYDRANENCEPHALY
MICROHYDRANENCEPHALY 		1 0 1 5.0E-02 0 0
CUI: C1969024
Disease: CARDIOMYOPATHY, DILATED, 1X
CARDIOMYOPATHY, DILATED, 1X 		1 0 1 5.0E-02 0 0
CUI: C1969029
Disease: Lissencephaly 3
Lissencephaly 3 		1 0 1 5.0E-02 0 0
CUI: C1969040
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M 		1 0 1 5.0E-02 0 0
CUI: C3150411
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 		1 0 1 5.0E-02 0 0
CUI: C3150413
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 		1 0 1 5.0E-02 0 0
CUI: C3150414
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 		1 0 1 5.0E-02 0 0
CUI: C3150418
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 		1 0 1 5.0E-02 0 0
CUI: C3151184
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9 		1 0 1 5.0E-02 0 0
CUI: C3151461
Disease: LISSENCEPHALY 4
LISSENCEPHALY 4 		1 0 1 5.0E-02 0 0
CUI: C3552236
Disease: CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7 		1 0 1 5.0E-02 0 0
CUI: C3553331
Disease: Subcortical heterotopia
Subcortical heterotopia 		1 0 1 5.0E-02 0 0
CUI: C4016970
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5 		1 0 1 5.0E-02 0 0
CUI: C4022651
Disease: Reduced muscle fiber merosin
Reduced muscle fiber merosin 		1 0 1 5.0E-02 0 0
CUI: C4023352
Disease: Abnormality of higher mental function
Abnormality of higher mental function 		1 0 1 5.0E-02 0 0
CUI: C4023757
Disease: Abnormal dura mater morphology
Abnormal dura mater morphology 		1 0 1 5.0E-02 0 0
CUI: C4024959
Disease: Frontoparietal cortical dysplasia
Frontoparietal cortical dysplasia 		1 0 1 5.0E-02 0 0
CUI: C4225269
Disease: CRANIOSYNOSTOSIS 6
CRANIOSYNOSTOSIS 6 		1 0 1 5.0E-02 0 0
CUI: C4225291
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9 		1 0 1 5.0E-02 0 0
CUI: C4225359
Disease: LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA
LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA 		1 0 1 5.0E-02 0 0
CUI: C4310646
Disease: LISSENCEPHALY 8
LISSENCEPHALY 8 		1 0 1 5.0E-02 0 0