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 2.0E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 2.0E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 2.0E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.0E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 4.0E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 2.0E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 2.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.0E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.0E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 3 6.0E-03
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 1 2.7E-04 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI
35 0 1 2.7E-04 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 2.7E-04 0 0
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination
32 0 1 2.7E-04 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea
31 0 1 2.7E-04 0 0
CUI: C1844562
Disease: Medial flaring of the eyebrow
Medial flaring of the eyebrow
28 0 1 2.7E-04 0 0
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
24 0 1 2.7E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome
21 0 1 2.7E-04 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress
21 0 1 2.7E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia
21 0 1 2.7E-04 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome
20 0 1 2.7E-04 0 0
Juvenile amyotrophic lateral sclerosis
20 0 1 2.7E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes
19 0 1 2.7E-04 0 0
CUI: C0457133
Disease: Muscle eye brain disease
Muscle eye brain disease
19 0 1 2.7E-04 0 0
Congenital Myasthenic Syndromes, Presynaptic
19 0 1 2.7E-04 0 0