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: C0009398
Disease: Color vision defect
Color vision defect 		0 4 0 0 2 2.8E-03
CUI: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.4E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 1 0 0 1 1.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.4E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.4E-03
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		0 4 0 0 1 1.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 1.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 2 0 0 1 1.4E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		0 1 0 0 1 1.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.8E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 1.4E-03
CUI: C0860602
Disease: Anxious personality
Anxious personality 		0 2 0 0 1 1.4E-03
CUI: C0865791
Disease: Obstructive bronchitis
Obstructive bronchitis 		0 1 0 0 1 1.4E-03
CUI: C1275149
Disease: Multiple skin tags
Multiple skin tags 		0 1 0 0 1 1.4E-03
CUI: C1868512
Disease: Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 		0 2 0 0 2 2.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.4E-03
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		34 0 1 5.7E-04 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly 		25 0 1 5.7E-04 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		20 0 1 5.7E-04 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		19 0 1 5.7E-04 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		19 0 1 5.7E-04 0 0
CUI: C0034345
Disease: Pyruvate Dehydrogenase Complex Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease 		18 0 1 5.7E-04 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		18 0 1 5.7E-04 0 0
CUI: C3160738
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D2
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 		18 0 1 5.7E-04 0 0
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		18 0 1 5.7E-04 0 0