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: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 2.3E-03 0 0
CUI: C0238013
Disease: Invasive aspergillosis
Invasive aspergillosis
59 0 1 2.3E-03 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 1 2.3E-03 0 0
Familial thoracic aortic aneurysm and aortic dissection
59 0 1 2.3E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
58 0 1 2.3E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction
57 0 1 2.3E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum
57 0 1 2.3E-03 0 0
CUI: C1866730
Disease: Rhizomelia
Rhizomelia
57 0 1 2.3E-03 0 0
CUI: C4022018
Disease: Telangiectasia of the skin
Telangiectasia of the skin
56 0 1 2.3E-03 0 0
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency
56 0 1 2.3E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
55 0 1 2.3E-03 0 0
Adverse effects, not elsewhere classified
55 0 1 2.3E-03 0 0
Abnormality of pelvic girdle bone morphology
55 0 1 2.3E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign
54 0 1 2.3E-03 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
54 0 1 2.3E-03 0 0
CUI: C0751291
Disease: Desmoplastic Medulloblastoma
Desmoplastic Medulloblastoma
54 0 1 2.3E-03 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 2.3E-03 0 0
CUI: C0221232
Disease: Welts
Welts
53 0 1 2.4E-03 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia
53 0 1 2.4E-03 0 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput
53 0 1 2.4E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis
52 0 1 2.4E-03 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris
52 0 1 2.4E-03 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly
51 0 1 2.4E-03 0 0
CUI: C0455988
Disease: Hydrops Fetalis, Non-Immune
Hydrops Fetalis, Non-Immune
51 0 1 2.4E-03 0 0
CUI: C0013592
Disease: Ectropion
Ectropion
50 0 1 2.4E-03 0 0