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 2.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.1E-02
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 2.1E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 2.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.0E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.1E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 4.3E-02
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 1.1E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		53 0 1 1.1E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		45 0 1 1.2E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		45 0 1 1.2E-03 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies 		44 0 1 1.2E-03 0 0
CUI: C0858600
Disease: Taste sweet
Taste sweet 		41 0 1 1.2E-03 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 0 1 1.2E-03 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		35 0 1 1.2E-03 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		34 0 1 1.2E-03 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		34 0 1 1.2E-03 0 0
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome 		33 0 1 1.2E-03 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		33 0 1 1.2E-03 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay 		33 0 1 1.2E-03 0 0
CUI: C0920296
Disease: Developmental reading disorder
Developmental reading disorder 		33 0 1 1.2E-03 0 0
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder 		31 0 1 1.2E-03 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		29 0 1 1.2E-03 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 1 1.2E-03 0 0