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: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		33 0 24 0.63 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 21 0.18 0 0
CUI: C4021020
Disease: Non-midline cleft lip
Non-midline cleft lip 		16 0 5 0.12 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology 		35 0 7 0.12 0 0
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney 		69 0 10 0.11 0 0
CUI: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome 		3 0 3 0.10 0 0
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome 		3 0 3 0.10 0 0
CUI: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		5 0 3 9.7E-02 0 0
CUI: C1720275
Disease: Gonadotropin releasing factor deficiency
Gonadotropin releasing factor deficiency 		5 0 3 9.7E-02 0 0
CUI: C0238210
Disease: Malrotation of kidney
Malrotation of kidney 		8 0 3 8.8E-02 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 3 8.8E-02 0 0
CUI: C1968949
Disease: Cakut
Cakut 		72 0 8 8.6E-02 0 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		9 0 3 8.6E-02 0 0
CUI: C1865279
Disease: Fetal polyuria
Fetal polyuria 		10 0 3 8.3E-02 0 0
CUI: C0037205
Disease: Sirenomelia
Sirenomelia 		11 0 3 8.1E-02 0 0
CUI: C0853877
Disease: Fistula of genitourinary tract
Fistula of genitourinary tract 		11 0 3 8.1E-02 0 0
CUI: C1865292
Disease: Nonketotic hypoglycemia
Nonketotic hypoglycemia 		11 0 3 8.1E-02 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 3 7.9E-02 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern 		15 0 3 7.3E-02 0 0
CUI: C1321884
Disease: Atresia of vagina
Atresia of vagina 		16 0 3 7.1E-02 0 0
CUI: C1839730
Disease: Prieto X-linked mental retardation syndrome
Prieto X-linked mental retardation syndrome 		16 0 3 7.1E-02 0 0
CUI: C0238441
Disease: Subglottic stenosis
Subglottic stenosis 		17 0 3 7.0E-02 0 0
CUI: C0266292
Disease: Congenital anomaly of the kidney
Congenital anomaly of the kidney 		63 0 6 7.0E-02 0 0
CUI: C4025250
Disease: Abnormal sacrum morphology
Abnormal sacrum morphology 		17 0 3 7.0E-02 0 0
CUI: C0332909
Disease: Congenital unilateral absence
Congenital unilateral absence 		2 0 2 6.9E-02 0 0