Source: BEFREE ×
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: C0036344
Disease: Schizophrenia, Catatonic
Schizophrenia, Catatonic 		8 0 1 1.6E-04 0 0
CUI: C0043168
Disease: Whooping cough due to unspecified organism
Whooping cough due to unspecified organism 		8 0 1 1.6E-04 0 0
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood 		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: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3 		8 0 1 1.6E-04 0 0
CUI: C2025392
Disease: Polar cataract
Polar cataract 		8 0 1 1.6E-04 0 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		7 0 1 1.6E-04 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		7 0 1 1.6E-04 0 0
CUI: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		7 0 1 1.6E-04 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 0 1 1.6E-04 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 1 1.6E-04 0 0
CUI: C1850055
Disease: PEHO syndrome
PEHO syndrome 		7 0 1 1.6E-04 0 0
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder) 		7 0 1 1.6E-04 0 0
CUI: C1850808
Disease: Miyoshi myopathy
Miyoshi myopathy 		7 0 1 1.6E-04 0 0
CUI: C1858477
Disease: Epilepsy, Partial, with Variable Foci
Epilepsy, Partial, with Variable Foci 		7 0 1 1.6E-04 0 0
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		7 0 1 1.6E-04 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		7 0 1 1.6E-04 0 0
CUI: C3150852
Disease: EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION
EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION 		7 0 1 1.6E-04 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 1 1.6E-04 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 1.6E-04 0 0
CUI: C4518639
Disease: Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures 		7 0 1 1.6E-04 0 0
CUI: C4551973
Disease: Miyoshi Muscular Dystrophy 1
Miyoshi Muscular Dystrophy 1 		7 0 1 1.6E-04 0 0
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia 		6 0 1 1.6E-04 0 0
CUI: C0162628
Disease: Skin Diseases, Viral
Skin Diseases, Viral 		6 0 1 1.6E-04 0 0
CUI: C0175683
Disease: Citrullinemia
Citrullinemia 		6 0 1 1.6E-04 0 0