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: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy 		1 0 1 8.3E-02 0 0
CUI: C1291575
Disease: Deficiency of citrate(si)-synthase
Deficiency of citrate(si)-synthase 		1 0 1 8.3E-02 0 0
CUI: C3150972
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE ID
NEUROPATHY, HEREDITARY SENSORY, TYPE ID 		1 0 1 8.3E-02 0 0
CUI: C4025809
Disease: Penetrating foot ulcers
Penetrating foot ulcers 		1 0 1 8.3E-02 0 0
CUI: C4540434
Disease: COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA
COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA 		1 0 1 8.3E-02 0 0
CUI: C1833222
Disease: Autoamputation
Autoamputation 		2 0 1 7.7E-02 0 0
CUI: C1970009
Disease: SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE 		2 0 1 7.7E-02 0 0
CUI: C0543641
Disease: Megaloblastic anemia, secondary
Megaloblastic anemia, secondary 		3 0 1 7.1E-02 0 0
CUI: C1864975
Disease: Osteomyelitis leading to amputation due to slow healing fractures
Osteomyelitis leading to amputation due to slow healing fractures 		3 0 1 7.1E-02 0 0
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 0 1 7.1E-02 0 0
CUI: C4021375
Disease: Attached earlobe
Attached earlobe 		3 0 1 7.1E-02 0 0
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 0 1 7.1E-02 0 0
CUI: C0020453
Disease: Hyperesthesia
Hyperesthesia 		6 0 1 5.9E-02 0 0
CUI: C1960883
Disease: Spina bifida aperta of cervical spine
Spina bifida aperta of cervical spine 		6 0 1 5.9E-02 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4 		7 0 1 5.6E-02 0 0
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin 		7 0 1 5.6E-02 0 0
CUI: C1866558
Disease: Neural tube defect, folate-sensitive
Neural tube defect, folate-sensitive 		8 0 1 5.3E-02 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 1 5.0E-02 0 0
CUI: C1836527
Disease: Distal sensory impairment of all modalities
Distal sensory impairment of all modalities 		9 0 1 5.0E-02 0 0
CUI: C0341395
Disease: Perianal Crohn's disease
Perianal Crohn's disease 		10 0 1 4.8E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 1 4.8E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 4.3E-02 0 0
CUI: C0600298
Disease: Periodontosis
Periodontosis 		12 0 1 4.3E-02 0 0
CUI: C0265344
Disease: Donohue Syndrome
Donohue Syndrome 		15 0 1 3.8E-02 0 0
CUI: C0004093
Disease: Asthenia
Asthenia 		16 0 1 3.7E-02 0 0