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 1.1E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.1E-03
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 1.1E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.1E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.1E-03
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 1.1E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 1.1E-03
CUI: C1456582
Disease: Vision Impairment and Blindness
Vision Impairment and Blindness 		0 1 0 0 1 1.1E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 1.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 3 3.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.1E-03
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism 		0 2 0 0 1 1.1E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 1.1E-03
CUI: C0919909
Disease: Tonic clonic movements
Tonic clonic movements 		22 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: C0037231
Disease: Sjogren-Larsson Syndrome
Sjogren-Larsson Syndrome 		20 0 1 5.0E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		18 0 1 5.0E-04 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		18 0 1 5.0E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		17 0 1 5.0E-04 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 5.0E-04 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		16 0 1 5.0E-04 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 0 1 5.0E-04 0 0
CUI: C1266128
Disease: Ossifying fibromyxoid tumor
Ossifying fibromyxoid tumor 		16 0 1 5.0E-04 0 0
CUI: C1318881
Disease: Vancomycin intermediate staphylococcus aureus infection
Vancomycin intermediate staphylococcus aureus infection 		16 0 1 5.0E-04 0 0
CUI: C1839730
Disease: Prieto X-linked mental retardation syndrome
Prieto X-linked mental retardation syndrome 		16 0 1 5.0E-04 0 0