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: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 1.0E-01 0 0
CUI: C2673482
Disease: Increased susceptibility to schizophrenia
Increased susceptibility to schizophrenia 		1 0 1 1.0E-01 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 1.0E-01 0 0
CUI: C2750784
Disease: SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 1.0E-01 0 0
CUI: C2827432
Disease: Bile Acid Synthesis Defect
Bile Acid Synthesis Defect 		1 0 1 1.0E-01 0 0
CUI: C3150644
Disease: BRACHYDACTYLY, TYPE E2
BRACHYDACTYLY, TYPE E2 		1 0 1 1.0E-01 0 0
CUI: C3542549
Disease: SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C4016483
Disease: PELIZAEUS-MERZBACHER DISEASE, CONNATAL
PELIZAEUS-MERZBACHER DISEASE, CONNATAL 		1 0 1 1.0E-01 0 0
CUI: C4016484
Disease: PELIZAEUS-MERZBACHER DISEASE, MILD
PELIZAEUS-MERZBACHER DISEASE, MILD 		1 0 1 1.0E-01 0 0
CUI: C4021852
Disease: Reduction of oligodendroglia
Reduction of oligodendroglia 		1 0 1 1.0E-01 0 0
CUI: C4304715
Disease: Congenital bile acid synthesis defect type 3
Congenital bile acid synthesis defect type 3 		1 0 1 1.0E-01 0 0
CUI: C4747646
Disease: LYMPHATIC MALFORMATION 3
LYMPHATIC MALFORMATION 3 		1 0 1 1.0E-01 0 0
CUI: C0278184
Disease: Scanning speech
Scanning speech 		13 0 2 9.5E-02 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord 		13 0 2 9.5E-02 0 0
CUI: C0265312
Disease: Brachydactyly syndrome type E
Brachydactyly syndrome type E 		2 0 1 9.1E-02 0 0
CUI: C0333457
Disease: Segmental demyelination
Segmental demyelination 		2 0 1 9.1E-02 0 0
CUI: C0346203
Disease: Cervical Adenocarcinoma In Situ
Cervical Adenocarcinoma In Situ 		2 0 1 9.1E-02 0 0
CUI: C0700110
Disease: Carcinoma bone
Carcinoma bone 		2 0 1 9.1E-02 0 0
CUI: C0751716
Disease: Adult Neuroaxonal Dystrophy
Adult Neuroaxonal Dystrophy 		2 0 1 9.1E-02 0 0
CUI: C0751717
Disease: Juvenile Neuroaxonal Dystrophy
Juvenile Neuroaxonal Dystrophy 		2 0 1 9.1E-02 0 0
CUI: C0751718
Disease: Late Infantile Neuroaxonal Dystrophy
Late Infantile Neuroaxonal Dystrophy 		2 0 1 9.1E-02 0 0
CUI: C0751914
Disease: Adult Pelizaeus-Merzbacher Disease
Adult Pelizaeus-Merzbacher Disease 		2 0 1 9.1E-02 0 0
CUI: C0751915
Disease: Pelizaeus-Merzbacher Disease, Atypical
Pelizaeus-Merzbacher Disease, Atypical 		2 0 1 9.1E-02 0 0
CUI: C0751916
Disease: Classic Pelizaeus-Merzbacher Disease
Classic Pelizaeus-Merzbacher Disease 		2 0 1 9.1E-02 0 0
CUI: C0751917
Disease: Pelizaeus-Merzbacher Disease, Transitional
Pelizaeus-Merzbacher Disease, Transitional 		2 0 1 9.1E-02 0 0