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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 1 0 0 1 6.5E-03
CUI: C0026884
Disease: Mutism
Mutism 		0 2 0 0 1 6.5E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 6.5E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 6.5E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 6.4E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 6.5E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.5E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 6.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 6.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.5E-03
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 6.5E-03
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.1E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		45 0 1 1.1E-03 0 0
CUI: C0239337
Disease: Deformity of limb
Deformity of limb 		37 0 1 1.1E-03 0 0
CUI: C0267446
Disease: Acute gastroenteritis
Acute gastroenteritis 		36 0 1 1.1E-03 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		34 0 1 1.1E-03 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		31 0 1 1.1E-03 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 1 1.1E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		29 0 1 1.1E-03 0 0
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos 		29 0 1 1.1E-03 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 1 1.1E-03 0 0
CUI: C0175694
Disease: Smith-Lemli-Opitz Syndrome
Smith-Lemli-Opitz Syndrome 		28 0 1 1.1E-03 0 0
CUI: C0266468
Disease: Congenital pontocerebellar hypoplasia
Congenital pontocerebellar hypoplasia 		28 0 1 1.1E-03 0 0
CUI: C2732267
Disease: Auditory neuropathy spectrum disorder
Auditory neuropathy spectrum disorder 		28 0 1 1.1E-03 0 0