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: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 4 4.7E-02
CUI: C1720863
Disease: Congenital Generalized Lipodystrophy Type 2
Congenital Generalized Lipodystrophy Type 2 		0 30 0 0 1 1.1E-02
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 9.2E-04 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		70 0 1 9.5E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 9.6E-04 0 0
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		56 0 1 9.6E-04 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 0 1 9.6E-04 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 9.6E-04 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 9.6E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 9.7E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 9.7E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 9.7E-04 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 0 1 9.7E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 9.7E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 9.7E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 9.7E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 9.7E-04 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 9.7E-04 0 0
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		41 0 1 9.8E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 9.8E-04 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 1 9.8E-04 0 0
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		41 0 1 9.8E-04 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 9.8E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 9.8E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 9.8E-04 0 0