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 4.1E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 3 0 0 1 4.0E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 4.1E-03
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 4.0E-03
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 1 0 0 1 4.1E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 4.1E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 4.0E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 4.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 4.0E-03
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 4.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 4.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.1E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 4.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 8.1E-03
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		57 0 1 3.9E-04 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		22 0 1 3.9E-04 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		22 0 1 3.9E-04 0 0
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		22 0 1 3.9E-04 0 0
CUI: C0272002
Disease: alpha^0^ Thalassemia
alpha^0^ Thalassemia 		21 0 1 3.9E-04 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 1 3.9E-04 0 0
CUI: C0043528
Disease: Zoonoses
Zoonoses 		19 0 1 3.9E-04 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		19 0 1 3.9E-04 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		18 0 1 3.9E-04 0 0
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		17 0 1 3.9E-04 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 1 3.9E-04 0 0