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: C4022771
Disease: Decreased thalamic volume
Decreased thalamic volume 		7 0 1 9.8E-05 0 0
CUI: C4024905
Disease: Abnormality of the pons
Abnormality of the pons 		7 0 1 9.8E-05 0 0
CUI: C0029516
Disease: Other and unspecified reactive psychosis
Other and unspecified reactive psychosis 		6 0 1 9.8E-05 0 0
CUI: C0268534
Disease: Prolinuria
Prolinuria 		6 0 1 9.8E-05 0 0
CUI: C0269133
Disease: Urethrovaginal fistula
Urethrovaginal fistula 		6 0 1 9.8E-05 0 0
CUI: C0270851
Disease: Benign neonatal epilepsy
Benign neonatal epilepsy 		6 0 1 9.8E-05 0 0
CUI: C0271934
Disease: Congenital dyserythropoietic anemia, type III
Congenital dyserythropoietic anemia, type III 		6 0 1 9.8E-05 0 0
CUI: C0585539
Disease: X-Linked Infantile Nystagmus
X-Linked Infantile Nystagmus 		6 0 1 9.8E-05 0 0
CUI: C1853296
Disease: SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3
SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3 		6 0 1 9.8E-05 0 0
CUI: C1858424
Disease: Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency 		6 0 1 9.8E-05 0 0
CUI: C2751052
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 		6 0 1 9.8E-05 0 0
CUI: C3150412
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 		6 0 1 9.8E-05 0 0
CUI: C3150415
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 		6 0 1 9.8E-05 0 0
CUI: C4020800
Disease: Decreased activity of mitochondrial complex IV
Decreased activity of mitochondrial complex IV 		6 0 1 9.8E-05 0 0
CUI: C4022989
Disease: Absent outer dynein arms
Absent outer dynein arms 		6 0 1 9.8E-05 0 0
CUI: C4552662
Disease: Rhinorrhea, CTCAE
Rhinorrhea, CTCAE 		6 0 1 9.8E-05 0 0
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		5 7 1 9.8E-05 1 6.1E-04
CUI: C0270854
Disease: Symptomatic Generalized Epilepsy
Symptomatic Generalized Epilepsy 		5 0 1 9.8E-05 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 1 9.8E-05 0 0
CUI: C0345427
Disease: Woolly hair, congenital
Woolly hair, congenital 		5 0 1 9.8E-05 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction 		5 0 1 9.8E-05 0 0
CUI: C0432195
Disease: Short rib dysplasia
Short rib dysplasia 		5 0 1 9.8E-05 0 0
CUI: C0520933
Disease: Abnormal spermatogenesis
Abnormal spermatogenesis 		5 0 1 9.8E-05 0 0
CUI: C1456276
Disease: Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome)
Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome) 		5 0 1 9.8E-05 0 0
CUI: C1619634
Disease: erythrocyte sedimentation rate result
erythrocyte sedimentation rate result 		5 0 1 9.8E-05 0 0