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: C4024645
Disease: Incomplete male pseudohermaphroditism
Incomplete male pseudohermaphroditism 		1 0 1 0.11 0 0
CUI: C4025328
Disease: Abnormality of alkaline phosphatase activity
Abnormality of alkaline phosphatase activity 		1 0 1 0.11 0 0
CUI: C4025829
Disease: Abnormality of the breast
Abnormality of the breast 		1 0 1 0.11 0 0
CUI: C4512053
Disease: 4p16.3 microduplication syndrome
4p16.3 microduplication syndrome 		1 0 1 0.11 0 0
CUI: C4518822
Disease: 17q12 microdeletion syndrome
17q12 microdeletion syndrome 		1 0 1 0.11 0 0
CUI: C4520921
Disease: Stage 0 Gastric Cancer AJCC v6 and v7
Stage 0 Gastric Cancer AJCC v6 and v7 		1 0 1 0.11 0 0
CUI: C4707448
Disease: Ring chromosome 2 syndrome
Ring chromosome 2 syndrome 		1 0 1 0.11 0 0
CUI: C0265931
Disease: Persistent left superior vena cava
Persistent left superior vena cava 		2 0 1 1.0E-01 0 0
CUI: C0302246
Disease: Hexadactyly
Hexadactyly 		2 0 1 1.0E-01 0 0
CUI: C0332910
Disease: bilateral agenesis
bilateral agenesis 		2 0 1 1.0E-01 0 0
CUI: C0344963
Disease: Right hypoplastic heart syndrome
Right hypoplastic heart syndrome 		2 0 1 1.0E-01 0 0
CUI: C0795805
Disease: Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q 		2 0 1 1.0E-01 0 0
CUI: C1332582
Disease: Primary bone lymphoma
Primary bone lymphoma 		2 0 1 1.0E-01 0 0
CUI: C1542327
Disease: Fetus or newborn affected by alcohol transmitted via placenta or breast milk
Fetus or newborn affected by alcohol transmitted via placenta or breast milk 		2 0 1 1.0E-01 0 0
CUI: C1839707
Disease: AUTISM, SEVERE
AUTISM, SEVERE 		2 0 1 1.0E-01 0 0
CUI: C1840451
Disease: MULTICYSTIC RENAL DYSPLASIA, BILATERAL
MULTICYSTIC RENAL DYSPLASIA, BILATERAL 		2 0 1 1.0E-01 0 0
CUI: C1842464
Disease: Nablus mask-like facial syndrome
Nablus mask-like facial syndrome 		2 0 1 1.0E-01 0 0
CUI: C1862260
Disease: BPES type I
BPES type I 		2 1 2 0.22 1 1.1E-02
CUI: C1865644
Disease: Plantar Lipomatosis, Unusual Facies, and Developmental Delay
Plantar Lipomatosis, Unusual Facies, and Developmental Delay 		2 0 1 1.0E-01 0 0
CUI: C2609249
Disease: Ureterovesical junction obstruction
Ureterovesical junction obstruction 		2 0 1 1.0E-01 0 0
CUI: C2673888
Disease: Decreased numbers of nephrons
Decreased numbers of nephrons 		2 0 1 1.0E-01 0 0
CUI: C2674949
Disease: Chromosome 3q29 Deletion Syndrome
Chromosome 3q29 Deletion Syndrome 		2 0 1 1.0E-01 0 0
CUI: C2748932
Disease: Slanting of the palpebral fissure
Slanting of the palpebral fissure 		2 0 1 1.0E-01 0 0
CUI: C3280216
Disease: HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 		2 0 1 1.0E-01 0 0
CUI: C3281138
Disease: CHROMOSOME 17q12 DELETION SYNDROME
CHROMOSOME 17q12 DELETION SYNDROME 		2 0 1 1.0E-01 0 0