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 6.0E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 6.0E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.0E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 6.0E-03
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		0 1 0 0 1 6.0E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 6.0E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 6.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 6.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 5.9E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.0E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 6.0E-03
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		34 0 1 4.7E-04 0 0
CUI: C1852373
Disease: Mitochondrial encephalopathy
Mitochondrial encephalopathy 		26 0 1 4.8E-04 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		23 0 1 4.8E-04 0 0
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		23 0 1 4.8E-04 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		22 0 1 4.8E-04 0 0
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia 		20 0 1 4.8E-04 0 0
CUI: C3468114
Disease: Juvenile amyotrophic lateral sclerosis
Juvenile amyotrophic lateral sclerosis 		20 0 1 4.8E-04 0 0
CUI: C0085583
Disease: Choreoathetosis
Choreoathetosis 		19 0 1 4.8E-04 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		19 0 1 4.8E-04 0 0
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease 		17 0 1 4.8E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		17 0 1 4.8E-04 0 0
CUI: C0038017
Disease: Congenital spondylolisthesis
Congenital spondylolisthesis 		17 0 1 4.8E-04 0 0
CUI: C1335468
Disease: precancerous polyps
precancerous polyps 		17 0 1 4.8E-04 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 4.8E-04 0 0