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: C0014854
Disease: Esophageal diverticulum
Esophageal diverticulum 		1 0 1 3.7E-02 0 0
CUI: C0265729
Disease: Mesatipellic pelvis
Mesatipellic pelvis 		1 0 1 3.7E-02 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 3.7E-02 0 0
CUI: C0580550
Disease: Lymphocyte count abnormal
Lymphocyte count abnormal 		1 0 1 3.7E-02 0 0
CUI: C0747733
Disease: Polychondritis
Polychondritis 		1 0 1 3.7E-02 0 0
CUI: C0749794
Disease: Upper Extremity Deformities, Congenital
Upper Extremity Deformities, Congenital 		1 0 1 3.7E-02 0 0
CUI: C1333446
Disease: Esophageal Gastrointestinal Stromal Tumor
Esophageal Gastrointestinal Stromal Tumor 		1 0 1 3.7E-02 0 0
CUI: C1378512
Disease: Blast cell leukemia
Blast cell leukemia 		1 0 1 3.7E-02 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 23 1 3.7E-02 1 3.4E-02
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 3.7E-02 0 0
CUI: C1849762
Disease: Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia
Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia 		1 0 1 3.7E-02 0 0
CUI: C1858043
Disease: Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation
Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation 		1 0 1 3.7E-02 0 0
CUI: C1862083
Disease: Short 4th toe
Short 4th toe 		1 0 1 3.7E-02 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 3.7E-02 0 0
CUI: C1867000
Disease: Hypoplastic/absent/deformed radius
Hypoplastic/absent/deformed radius 		1 0 1 3.7E-02 0 0
CUI: C1867003
Disease: Axillary apocrine gland hypoplasia
Axillary apocrine gland hypoplasia 		1 0 1 3.7E-02 0 0
CUI: C2931001
Disease: Congenital disorder of glycosylation type 1G
Congenital disorder of glycosylation type 1G 		1 0 1 3.7E-02 0 0
CUI: C2931004
Disease: Congenital disorder of glycosylation type 1J
Congenital disorder of glycosylation type 1J 		1 0 1 3.7E-02 0 0
CUI: C2931010
Disease: Congenital disorder of glycosylation type 2E
Congenital disorder of glycosylation type 2E 		1 0 1 3.7E-02 0 0
CUI: C3280127
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 		1 0 1 3.7E-02 0 0
CUI: C3280168
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC 		1 19 1 3.7E-02 1 4.0E-02
CUI: C3280283
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 		1 37 1 3.7E-02 1 2.3E-02
CUI: C3553645
Disease: MYASTHENIC SYNDROME, CONGENITAL, 13
MYASTHENIC SYNDROME, CONGENITAL, 13 		1 0 1 3.7E-02 0 0
CUI: C3553999
Disease: PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) 		1 0 1 3.7E-02 0 0
CUI: C3806688
Disease: Solute carrier family 35 member A2 congenital disorder of glycosylation
Solute carrier family 35 member A2 congenital disorder of glycosylation 		1 0 1 3.7E-02 0 0