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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 2 2.2E-02
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0 95 0 0 1 5.6E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 1.2E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 2.4E-02
CUI: C3553462
Disease: INFLUENZA, SEVERE, SUSCEPTIBILITY TO
INFLUENZA, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 1.2E-02
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 1.2E-02
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		284 0 1 1.4E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 1.5E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 1.6E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 1.6E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 1.7E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 1.7E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 1.7E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.7E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 1.7E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 1.7E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation 		160 0 1 1.7E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		160 0 1 1.7E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia 		148 0 1 1.8E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency 		148 0 1 1.8E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		148 0 1 1.8E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 1.8E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 1.8E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial 		142 0 1 1.8E-03 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 1 1.8E-03 0 0