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: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0266507
Disease: Myeloschisis
Myeloschisis 		1 0 1 7.7E-02 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome 		1 0 1 7.7E-02 0 0
CUI: C0281334
Disease: Adult Papillary Meningioma
Adult Papillary Meningioma 		1 0 1 7.7E-02 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 4 7.7E-02 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1836437
Disease: B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations 		1 0 1 7.7E-02 0 0
CUI: C1836485
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1850395
Disease: Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive 		1 0 1 7.7E-02 0 0
CUI: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 7.7E-02 0 0
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		1 0 1 7.7E-02 0 0
CUI: C1868514
Disease: Diffuse leukoencephalopathy
Diffuse leukoencephalopathy 		1 0 1 7.7E-02 0 0
CUI: C1868527
Disease: Decreased sweating due to autonomic dysfunction
Decreased sweating due to autonomic dysfunction 		1 0 1 7.7E-02 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 7.7E-02 0 0
CUI: C2827432
Disease: Bile Acid Synthesis Defect
Bile Acid Synthesis Defect 		1 0 1 7.7E-02 0 0
CUI: C2931844
Disease: Spinal muscular atrophy 4
Spinal muscular atrophy 4 		1 0 1 7.7E-02 0 0
CUI: C4015436
Disease: ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS
ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS 		1 0 1 7.7E-02 0 0
CUI: C4024914
Disease: Symmetric peripheral demyelination
Symmetric peripheral demyelination 		1 0 1 7.7E-02 0 0
CUI: C4073057
Disease: Color vision test abnormality
Color vision test abnormality 		1 0 1 7.7E-02 0 0
CUI: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3 		1 0 1 7.7E-02 0 0
CUI: C4225272
Disease: SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE 		1 0 1 7.7E-02 0 0
CUI: C4304715
Disease: Congenital bile acid synthesis defect type 3
Congenital bile acid synthesis defect type 3 		1 0 1 7.7E-02 0 0
CUI: C4310725
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B 		1 0 1 7.7E-02 0 0
CUI: C4310875
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2A 		1 0 1 7.7E-02 0 0
CUI: C4551776
Disease: RITSCHER-SCHINZEL SYNDROME 1
RITSCHER-SCHINZEL SYNDROME 1 		1 0 1 7.7E-02 0 0