Source: BEFREE ×
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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.2E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.2E-02
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 1.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-02
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1 		0 1 0 0 1 1.2E-02
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly 		25 0 1 4.0E-04 0 0
CUI: C3888090
Disease: Early onset torsion dystonia
Early onset torsion dystonia 		22 0 1 4.0E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		20 0 1 4.0E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 4.0E-04 0 0
CUI: C4317123
Disease: Myoclonic Seizures
Myoclonic Seizures 		20 0 1 4.0E-04 0 0
CUI: C0220669
Disease: Familial benign neonatal epilepsy
Familial benign neonatal epilepsy 		18 0 1 4.0E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		18 0 1 4.0E-04 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		18 0 1 4.0E-04 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 4.0E-04 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		16 0 1 4.0E-04 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		16 0 1 4.0E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		16 0 1 4.0E-04 0 0
CUI: C4551508
Disease: Dominant hereditary optic atrophy
Dominant hereditary optic atrophy 		16 0 1 4.0E-04 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		15 0 1 4.0E-04 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 1 4.0E-04 0 0
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		14 0 1 4.0E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		14 0 1 4.0E-04 0 0
CUI: C0266006
Disease: Pili torti-deafness syndrome
Pili torti-deafness syndrome 		14 0 1 4.0E-04 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		14 0 1 4.0E-04 0 0
CUI: C0685838
Disease: Gonadal dysgenesis XX type deafness
Gonadal dysgenesis XX type deafness 		14 0 1 4.0E-04 0 0