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: C0043168
Disease: Whooping cough due to unspecified organism
Whooping cough due to unspecified organism 		8 0 1 2.0E-04 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism 		8 0 1 2.0E-04 0 0
CUI: C0268540
Disease: HHH syndrome
HHH syndrome 		8 0 1 2.0E-04 0 0
CUI: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 1 2.0E-04 0 0
CUI: C0406740
Disease: Kohlschutter Tonz syndrome
Kohlschutter Tonz syndrome 		8 0 1 2.0E-04 0 0
CUI: C0410198
Disease: Proximal myopathy
Proximal myopathy 		8 0 1 2.0E-04 0 0
CUI: C0796013
Disease: Zimmerman Laband syndrome
Zimmerman Laband syndrome 		8 0 1 2.0E-04 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		8 0 1 2.0E-04 0 0
CUI: C1849930
Disease: Persistent Mullerian duct syndrome
Persistent Mullerian duct syndrome 		8 0 1 2.0E-04 0 0
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2 		8 0 1 2.0E-04 0 0
CUI: C3280641
Disease: Decreased serum complement C4b
Decreased serum complement C4b 		8 0 1 2.0E-04 0 0
CUI: C3494361
Disease: Prodromal Stage
Prodromal Stage 		8 0 1 2.0E-04 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		8 0 1 2.0E-04 0 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		7 0 1 2.0E-04 0 0
CUI: C0022797
Disease: Adult Neuronal Ceroid Lipofuscinosis
Adult Neuronal Ceroid Lipofuscinosis 		7 0 1 2.0E-04 0 0
CUI: C0158995
Disease: Congenital anemia
Congenital anemia 		7 0 1 2.0E-04 0 0
CUI: C0270962
Disease: Multi-core congenital myopathy
Multi-core congenital myopathy 		7 0 1 2.0E-04 0 0
CUI: C0748351
Disease: respiratory compensation
respiratory compensation 		7 0 1 2.0E-04 0 0
CUI: C0751229
Disease: Hypersomnolence
Hypersomnolence 		7 0 1 2.0E-04 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		7 0 1 2.0E-04 0 0
CUI: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		7 0 1 2.0E-04 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 1 2.0E-04 0 0
CUI: C1970209
Disease: Alzheimer Disease 12
Alzheimer Disease 12 		7 0 1 2.0E-04 0 0
CUI: C3281160
Disease: EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2 		7 0 1 2.0E-04 0 0
CUI: C3665342
Disease: Progressive Cone Dystrophy
Progressive Cone Dystrophy 		7 0 1 2.0E-04 0 0