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 6.5E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 6.5E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 6.5E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 6.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 6.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 6.4E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 6.5E-03
Philadelphia positive acute lymphocytic leukaemia
0 1 0 0 1 6.5E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
131 0 1 1.0E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 1.0E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
82 0 1 1.1E-03 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera
70 0 1 1.1E-03 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 1.1E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly
62 0 1 1.1E-03 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes
61 0 1 1.1E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 1.1E-03 0 0
CUI: C3275417
Disease: Ragged-red muscle fibers
Ragged-red muscle fibers
59 0 1 1.1E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 1 1.1E-03 0 0
CUI: C0040485
Disease: Torticollis
Torticollis
55 0 1 1.1E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 1.1E-03 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia
53 0 1 1.1E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs
51 0 1 1.1E-03 0 0
CUI: C0426789
Disease: Short thorax
Short thorax
51 0 1 1.1E-03 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 1 1.1E-03 0 0
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis
50 0 1 1.1E-03 0 0