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: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		10 0 5 0.50 0 0
CUI: C4721916
Disease: HMSN Type V
HMSN Type V 		7 0 4 0.50 0 0
CUI: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 0.20 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 0.20 0 0
CUI: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 0.20 0 0
CUI: C2673482
Disease: Increased susceptibility to schizophrenia
Increased susceptibility to schizophrenia 		1 0 1 0.20 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 0.20 0 0
CUI: C2827432
Disease: Bile Acid Synthesis Defect
Bile Acid Synthesis Defect 		1 0 1 0.20 0 0
CUI: C3542549
Disease: SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE 		1 0 1 0.20 0 0
CUI: C4016483
Disease: PELIZAEUS-MERZBACHER DISEASE, CONNATAL
PELIZAEUS-MERZBACHER DISEASE, CONNATAL 		1 0 1 0.20 0 0
CUI: C4016484
Disease: PELIZAEUS-MERZBACHER DISEASE, MILD
PELIZAEUS-MERZBACHER DISEASE, MILD 		1 0 1 0.20 0 0
CUI: C4021852
Disease: Reduction of oligodendroglia
Reduction of oligodendroglia 		1 0 1 0.20 0 0
CUI: C4304715
Disease: Congenital bile acid synthesis defect type 3
Congenital bile acid synthesis defect type 3 		1 0 1 0.20 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 4 0.19 0 0
CUI: C0333457
Disease: Segmental demyelination
Segmental demyelination 		2 0 1 0.17 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 2 0.17 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome 		9 0 2 0.17 0 0
CUI: C0751716
Disease: Adult Neuroaxonal Dystrophy
Adult Neuroaxonal Dystrophy 		2 0 1 0.17 0 0
CUI: C0751717
Disease: Juvenile Neuroaxonal Dystrophy
Juvenile Neuroaxonal Dystrophy 		2 0 1 0.17 0 0
CUI: C0751718
Disease: Late Infantile Neuroaxonal Dystrophy
Late Infantile Neuroaxonal Dystrophy 		2 0 1 0.17 0 0
CUI: C0751914
Disease: Adult Pelizaeus-Merzbacher Disease
Adult Pelizaeus-Merzbacher Disease 		2 0 1 0.17 0 0
CUI: C0751915
Disease: Pelizaeus-Merzbacher Disease, Atypical
Pelizaeus-Merzbacher Disease, Atypical 		2 0 1 0.17 0 0
CUI: C0751916
Disease: Classic Pelizaeus-Merzbacher Disease
Classic Pelizaeus-Merzbacher Disease 		2 0 1 0.17 0 0
CUI: C0751917
Disease: Pelizaeus-Merzbacher Disease, Transitional
Pelizaeus-Merzbacher Disease, Transitional 		2 0 1 0.17 0 0
CUI: C0751918
Disease: Cockayne-Pelizaeus-Merzbacher Disease
Cockayne-Pelizaeus-Merzbacher Disease 		2 0 1 0.17 0 0