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: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		15 0 1 2.7E-04 0 0
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL 		15 0 1 2.7E-04 0 0
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		15 0 1 2.7E-04 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		14 0 1 2.7E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		14 0 1 2.7E-04 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 1 2.7E-04 0 0
CUI: C2960129
Disease: Vanishing white matter disease
Vanishing white matter disease 		14 0 1 2.7E-04 0 0
CUI: C4021533
Disease: Severe sensorineural hearing impairment
Severe sensorineural hearing impairment 		14 0 1 2.7E-04 0 0
CUI: C1857299
Disease: RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL
RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL 		13 0 1 2.7E-04 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 1 2.7E-04 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy 		13 3 1 2.7E-04 1 1.7E-03
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease 		12 0 1 2.7E-04 0 0
CUI: C0085395
Disease: Ureaplasma Infections
Ureaplasma Infections 		12 0 1 2.7E-04 0 0
CUI: C0347959
Disease: Lactic acidemia
Lactic acidemia 		12 0 1 2.7E-04 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity 		12 0 1 2.7E-04 0 0
CUI: C0264722
Disease: Chronic congestive heart failure
Chronic congestive heart failure 		11 0 1 2.7E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		11 0 1 2.7E-04 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 1 2.7E-04 0 0
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
Familial dyshormonogenetic goiter 		11 0 1 2.7E-04 0 0
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome 		11 0 1 2.7E-04 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 1 2.7E-04 0 0
CUI: C0034091
Disease: Pulmonary Veno-Occlusive Disease (disorder)
Pulmonary Veno-Occlusive Disease (disorder) 		10 0 1 2.7E-04 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		10 0 1 2.7E-04 0 0
CUI: C0162292
Disease: External Ophthalmoplegia
External Ophthalmoplegia 		10 0 1 2.7E-04 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		10 0 1 2.7E-04 0 0