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 7.2E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 7.2E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 7.1E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 7.2E-03
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 7.2E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 7.2E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 7.2E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 7.2E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 7.1E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 7.2E-03
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 7.2E-03
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 1.4E-02
CUI: C2732267
Disease: Auditory neuropathy spectrum disorder
Auditory neuropathy spectrum disorder 		28 0 1 5.0E-04 0 0
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		26 0 1 5.0E-04 0 0
CUI: C1852373
Disease: Mitochondrial encephalopathy
Mitochondrial encephalopathy 		26 0 1 5.0E-04 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy 		23 0 1 5.0E-04 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		21 0 1 5.0E-04 0 0
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		21 0 1 5.0E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		20 0 1 5.0E-04 0 0
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia 		20 0 1 5.0E-04 0 0
CUI: C4317123
Disease: Myoclonic Seizures
Myoclonic Seizures 		20 0 1 5.0E-04 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		19 0 1 5.0E-04 0 0
CUI: C0220769
Disease: FG syndrome
FG syndrome 		19 0 1 5.0E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		19 0 1 5.0E-04 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		19 0 1 5.0E-04 0 0