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: C1848529
Disease: Hypoplasia of the pons
Hypoplasia of the pons
30 0 1 5.5E-04 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
30 0 1 5.5E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
30 0 1 5.5E-04 0 0
Abnormality of the intervertebral disk
30 0 1 5.5E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
29 0 1 5.5E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
29 0 1 5.5E-04 0 0
CUI: C0262374
Disease: Stricture of anus
Stricture of anus
28 0 1 5.5E-04 0 0
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
28 0 1 5.5E-04 0 0
Increased intramyocellular lipid droplets
27 0 1 5.5E-04 0 0
CUI: C4551936
Disease: Anal Stenosis, CTCAE
Anal Stenosis, CTCAE
27 0 1 5.5E-04 0 0
CUI: C1865186
Disease: Bell-shaped thorax
Bell-shaped thorax
26 0 1 5.5E-04 0 0
Prostate specific antigen measurement
25 0 1 5.5E-04 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome
25 0 1 5.5E-04 0 0
CUI: C0395837
Disease: Stenosis of external auditory canal
Stenosis of external auditory canal
25 0 1 5.5E-04 0 0
CUI: C1843392
Disease: Death in childhood
Death in childhood
25 0 1 5.5E-04 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
24 0 1 5.5E-04 0 0
CUI: C0233849
Disease: Personality Traits
Personality Traits
24 0 1 5.5E-04 0 0
CUI: C1842153
Disease: Irregular vertebral endplates
Irregular vertebral endplates
24 0 1 5.5E-04 0 0
Cytochrome C oxidase-negative muscle fibers
24 0 1 5.5E-04 0 0
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail
23 0 1 5.5E-04 0 0
CUI: C1857790
Disease: Thoracic scoliosis
Thoracic scoliosis
23 0 1 5.5E-04 0 0
CUI: C0036454
Disease: Scotoma
Scotoma
21 0 1 5.5E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome
21 0 1 5.5E-04 0 0
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome
21 0 1 5.5E-04 0 0
CUI: C0432028
Disease: Split foot
Split foot
21 0 1 5.5E-04 0 0