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 6.3E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 6.3E-04
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 6.3E-04
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 6.3E-04
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 6.3E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 1.3E-03
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 6.3E-04
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 6.3E-04
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 1 6.3E-04
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		0 1 0 0 1 6.3E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 6.3E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 6.3E-04
CUI: C3899405
Disease: Decreased Attention
Decreased Attention 		0 1 0 0 1 6.3E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 6.3E-04
CUI: C1842180
Disease: CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder) 		20 0 1 3.7E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		18 0 1 3.7E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		17 0 1 3.7E-04 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 3.7E-04 0 0
CUI: C3696898
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 		16 0 1 3.7E-04 0 0
CUI: C0016508
Disease: Congenital Foot Deformity
Congenital Foot Deformity 		15 0 1 3.7E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		14 0 1 3.7E-04 0 0
CUI: C0393541
Disease: Distal Spinal Muscular Atrophy
Distal Spinal Muscular Atrophy 		14 0 1 3.7E-04 0 0
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		14 0 1 3.7E-04 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 1 3.7E-04 0 0
CUI: C0007398
Disease: Catatonia
Catatonia 		13 0 1 3.7E-04 0 0