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: C0031946
Disease: Pinta
Pinta 		1 0 1 1.00 0 0
CUI: C4023135
Disease: Unilateral radial aplasia
Unilateral radial aplasia 		1 0 1 1.00 0 0
CUI: C4073210
Disease: Hyperplasia of the premaxilla
Hyperplasia of the premaxilla 		1 1 1 1.00 1 7.7E-02
CUI: C1853276
Disease: Deafness, Autosomal Recessive 28
Deafness, Autosomal Recessive 28 		2 15 1 0.50 1 3.7E-02
CUI: C2748932
Disease: Slanting of the palpebral fissure
Slanting of the palpebral fissure 		2 0 1 0.50 0 0
CUI: C4021375
Disease: Attached earlobe
Attached earlobe 		3 3 1 0.33 1 6.7E-02
CUI: C1275275
Disease: Spindle cell liposarcoma
Spindle cell liposarcoma 		4 0 1 0.25 0 0
CUI: C0040458
Disease: Unerupted tooth
Unerupted tooth 		5 0 1 0.20 0 0
CUI: C1838610
Disease: Aplasia of the 1st metacarpal
Aplasia of the 1st metacarpal 		5 0 1 0.20 0 0
CUI: C3805156
Disease: Chronic hepatitis C virus genotype 1
Chronic hepatitis C virus genotype 1 		8 0 1 0.12 0 0
CUI: C0266573
Disease: Congenital ptosis
Congenital ptosis 		10 0 1 1.0E-01 0 0
CUI: C0006009
Disease: Borderline intellectual disability
Borderline intellectual disability 		16 0 1 6.2E-02 0 0
CUI: C0745133
Disease: Isolated systolic hypertension
Isolated systolic hypertension 		22 0 1 4.5E-02 0 0
CUI: C1608426
Disease: Compensated cirrhosis
Compensated cirrhosis 		23 0 1 4.3E-02 0 0
CUI: C2940786
Disease: Thyroid Hormone Resistance Syndrome
Thyroid Hormone Resistance Syndrome 		25 5 1 4.0E-02 1 5.9E-02
CUI: C0346619
Disease: Malignant neoplasm of cardioesophageal junction of stomach
Malignant neoplasm of cardioesophageal junction of stomach 		26 0 1 3.8E-02 0 0
CUI: C1112160
Disease: Gastrooesophageal cancer
Gastrooesophageal cancer 		26 0 1 3.8E-02 0 0
CUI: C3714524
Disease: Fibromyxosarcoma
Fibromyxosarcoma 		33 0 1 3.0E-02 0 0
CUI: C0271980
Disease: beta^0^ Thalassemia
beta^0^ Thalassemia 		34 0 1 2.9E-02 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy 		38 0 1 2.6E-02 0 0
CUI: C0016689
Disease: Freckles
Freckles 		45 10 1 2.2E-02 1 4.5E-02
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 0 1 2.1E-02 0 0
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		51 0 1 2.0E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 1.9E-02 0 0
CUI: C1389018
Disease: Atrioventricular Septal Defect
Atrioventricular Septal Defect 		58 0 1 1.7E-02 0 0