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 1.1E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 1.1E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.1E-03
CUI: C0334328
Disease: Microfollicular adenoma
Microfollicular adenoma 		0 1 0 0 1 1.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.1E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 1.1E-03
CUI: C1318233
Disease: immunoglobulin G index
immunoglobulin G index 		0 4 0 0 1 1.1E-03
CUI: C1446147
Disease: IgG Index (procedure)
IgG Index (procedure) 		0 4 0 0 1 1.1E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.1E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.1E-03
CUI: C2930987
Disease: Paranasal sinus teratocarcinosarcoma (type)
Paranasal sinus teratocarcinosarcoma (type) 		0 1 0 0 1 1.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.1E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.1E-03
CUI: C2230441
Disease: Triceps weakness
Triceps weakness 		18 0 1 1.7E-04 0 0
CUI: C1839666
Disease: Calf muscle pseudohypertrophy
Calf muscle pseudohypertrophy 		17 0 1 1.7E-04 0 0
CUI: C1857632
Disease: Narrow palm
Narrow palm 		17 0 1 1.7E-04 0 0
CUI: C0036069
Disease: Saldino-Noonan Syndrome
Saldino-Noonan Syndrome 		16 0 1 1.7E-04 0 0
CUI: C1839071
Disease: Spermatogenic Failure, Nonobstructive, Y-Linked
Spermatogenic Failure, Nonobstructive, Y-Linked 		16 0 1 1.7E-04 0 0
CUI: C3279725
Disease: Hip flexor weakness
Hip flexor weakness 		16 0 1 1.7E-04 0 0
CUI: C2749688
Disease: Abnormal isoelectric focusing of serum transferrin
Abnormal isoelectric focusing of serum transferrin 		15 0 1 1.7E-04 0 0
CUI: C2936406
Disease: alpha-Dystroglycanopathies
alpha-Dystroglycanopathies 		15 0 1 1.7E-04 0 0
CUI: C4023786
Disease: Elevated levels of phytanic acid
Elevated levels of phytanic acid 		15 0 1 1.7E-04 0 0
CUI: C4025615
Disease: Decreased size of nerve terminals
Decreased size of nerve terminals 		15 0 1 1.7E-04 0 0
CUI: C1273957
Disease: Upper limb spasticity
Upper limb spasticity 		14 0 1 1.7E-04 0 0
CUI: C1303007
Disease: Brushfield spots
Brushfield spots 		14 0 1 1.7E-04 0 0