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: C0677600
Disease: Inspiratory stridor
Inspiratory stridor 		8 0 1 9.1E-02 0 0
CUI: C2750913
Disease: Neuronal loss in basal ganglia
Neuronal loss in basal ganglia 		8 0 1 9.1E-02 0 0
CUI: C2751584
Disease: Neurodegeneration Due To Cerebral Folate Transport Deficiency
Neurodegeneration Due To Cerebral Folate Transport Deficiency 		8 0 1 9.1E-02 0 0
CUI: C3711645
Disease: Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 		8 0 1 9.1E-02 0 0
CUI: C0748903
Disease: spinal cord involvement
spinal cord involvement 		9 0 1 8.3E-02 0 0
CUI: C1336030
Disease: Solid pseudopapillary tumour of the pancreas
Solid pseudopapillary tumour of the pancreas 		9 0 1 8.3E-02 0 0
CUI: C1709286
Disease: Null Cell Pituitary Gland Adenoma
Null Cell Pituitary Gland Adenoma 		9 0 1 8.3E-02 0 0
CUI: C1839858
Disease: Periventricular cysts
Periventricular cysts 		9 0 1 8.3E-02 0 0
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		9 0 1 8.3E-02 0 0
CUI: C4025711
Disease: Abnormal caudate nucleus morphology
Abnormal caudate nucleus morphology 		9 0 1 8.3E-02 0 0
CUI: C1282975
Disease: von Willebrand Disease, Type 2N
von Willebrand Disease, Type 2N 		10 0 1 7.7E-02 0 0
CUI: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness 		10 0 1 7.7E-02 0 0
CUI: C2750915
Disease: Basal ganglia gliosis
Basal ganglia gliosis 		10 0 1 7.7E-02 0 0
CUI: C3273010
Disease: Inflammatory Hepatocellular Adenoma
Inflammatory Hepatocellular Adenoma 		10 0 1 7.7E-02 0 0
CUI: C4021243
Disease: Abnormality of thalamus morphology
Abnormality of thalamus morphology 		10 0 1 7.7E-02 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology 		10 0 1 7.7E-02 0 0
CUI: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 1 7.1E-02 0 0
CUI: C1858427
Disease: Limited extraocular movements
Limited extraocular movements 		11 0 1 7.1E-02 0 0
CUI: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex 		11 0 1 7.1E-02 0 0
CUI: C0268119
Disease: Combined molybdoflavoprotein enzyme deficiency
Combined molybdoflavoprotein enzyme deficiency 		13 0 1 6.2E-02 0 0
CUI: C0338596
Disease: Spastic cerebral palsy
Spastic cerebral palsy 		13 0 1 6.2E-02 0 0
CUI: C0751197
Disease: Fulminant Hepatic Failure with Cerebral Edema
Fulminant Hepatic Failure with Cerebral Edema 		13 0 1 6.2E-02 0 0
CUI: C0751198
Disease: Hepatic Stupor
Hepatic Stupor 		13 0 1 6.2E-02 0 0
CUI: C0019147
Disease: Hepatic Coma
Hepatic Coma 		14 0 1 5.9E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 1 5.9E-02 0 0