Source: ALL
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 3.8E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.7E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.8E-03
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 7.7E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.8E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 2 7.7E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 3.8E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.8E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.8E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.8E-03
CUI: C4524071
Disease: Philadelphia positive acute lymphocytic leukaemia
Philadelphia positive acute lymphocytic leukaemia 		0 1 0 0 1 3.8E-03
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 1 8.7E-04 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 8.7E-04 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 8.7E-04 0 0
CUI: C0040485
Disease: Torticollis
Torticollis 		55 0 1 8.7E-04 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		55 0 1 8.7E-04 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 8.7E-04 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 1 8.7E-04 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination 		49 0 1 8.7E-04 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		48 0 1 8.7E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 8.7E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 8.8E-04 0 0
CUI: C1837402
Disease: Flat occiput
Flat occiput 		45 0 1 8.8E-04 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 1 8.8E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 8.8E-04 0 0