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: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1 		10 0 1 1.6E-04 0 0
CUI: C0700078
Disease: Decreased tendon reflex
Decreased tendon reflex 		10 0 1 1.6E-04 0 0
CUI: C1852372
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder) 		10 0 1 1.6E-04 0 0
CUI: C1859438
Disease: Frontalis muscle weakness
Frontalis muscle weakness 		10 0 1 1.6E-04 0 0
CUI: C4015098
Disease: Hypoglycosylation of alpha-dystroglycan
Hypoglycosylation of alpha-dystroglycan 		10 0 1 1.6E-04 0 0
CUI: C4022646
Disease: Reduced muscle fiber alpha dystroglycan
Reduced muscle fiber alpha dystroglycan 		10 0 1 1.6E-04 0 0
CUI: C0751267
Disease: Encephalopathy, Subacute Necrotizing, Infantile
Encephalopathy, Subacute Necrotizing, Infantile 		9 0 1 1.6E-04 0 0
CUI: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		9 0 1 1.6E-04 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly 		9 0 1 1.6E-04 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 1.6E-04 0 0
CUI: C1856655
Disease: Hypoplasia of olfactory tract
Hypoplasia of olfactory tract 		9 0 1 1.6E-04 0 0
CUI: C2748610
Disease: Progressive extrapyramidal movement disorder
Progressive extrapyramidal movement disorder 		9 0 1 1.6E-04 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 0 1 1.6E-04 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 1.6E-04 0 0
CUI: C4021262
Disease: Absent palmar crease
Absent palmar crease 		9 0 1 1.6E-04 0 0
CUI: C4021523
Disease: Upper limb amyotrophy
Upper limb amyotrophy 		9 0 1 1.6E-04 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility 		9 0 1 1.6E-04 0 0
CUI: C4273988
Disease: Benign adult familial myoclonic epilepsy
Benign adult familial myoclonic epilepsy 		9 0 1 1.6E-04 0 0
CUI: C0023772
Disease: Lipid Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors 		8 0 1 1.6E-04 0 0
CUI: C0263485
Disease: Clastothrix
Clastothrix 		8 0 1 1.6E-04 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 1 1.6E-04 0 0
CUI: C0268594
Disease: Glutaric aciduria
Glutaric aciduria 		8 0 1 1.6E-04 0 0
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		8 0 1 1.6E-04 0 0
CUI: C0852975
Disease: Congenital cerebellar ataxia
Congenital cerebellar ataxia 		8 0 1 1.6E-04 0 0
CUI: C1695776
Disease: Vertebral wedging
Vertebral wedging 		8 0 1 1.6E-04 0 0