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: C1839277
Disease: Submucous cleft lip
Submucous cleft lip 		2 0 2 0.33 0 0
CUI: C1839279
Disease: Six lumbar vertebrae
Six lumbar vertebrae 		2 0 2 0.33 0 0
CUI: C1839285
Disease: Two carpal ossification centers present at birth
Two carpal ossification centers present at birth 		2 0 2 0.33 0 0
CUI: C1839269
Disease: Duplication of renal pelvis
Duplication of renal pelvis 		3 0 2 0.29 0 0
CUI: C1839276
Disease: Broad secondary alveolar ridge
Broad secondary alveolar ridge 		4 0 2 0.25 0 0
CUI: C1866689
Disease: Short sacroiliac notch
Short sacroiliac notch 		4 0 2 0.25 0 0
CUI: C0796113
Disease: Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor 		7 0 2 0.18 0 0
CUI: C1850087
Disease: Narrow sacroiliac notch
Narrow sacroiliac notch 		7 0 2 0.18 0 0
CUI: C1862142
Disease: Short 2nd finger
Short 2nd finger 		7 0 2 0.18 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 0.17 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 1 1 0.17 1 0.50
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 0.17 0 0
CUI: C3275508
Disease: MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2 		1 0 1 0.17 0 0
CUI: C3806670
Disease: PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1 		1 0 1 0.17 0 0
CUI: C4015357
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 31
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 		1 29 1 0.17 1 3.3E-02
CUI: C4708498
Disease: PURA syndrome
PURA syndrome 		1 0 1 0.17 0 0
CUI: C4751570
Disease: Ferro-cerebro-cutaneous syndrome
Ferro-cerebro-cutaneous syndrome 		1 0 1 0.17 0 0
CUI: C0432055
Disease: Simple syndactyly of fingers - first web
Simple syndactyly of fingers - first web 		9 0 2 0.15 0 0
CUI: C4021539
Disease: Posterior helix pit
Posterior helix pit 		9 0 2 0.15 0 0
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome 		9 0 2 0.15 0 0
CUI: C0086774
Disease: Cold paroxysmal hemoglobinuria
Cold paroxysmal hemoglobinuria 		2 0 1 0.14 0 0
CUI: C0346183
Disease: Ovarian Embryonal Carcinoma
Ovarian Embryonal Carcinoma 		2 0 1 0.14 0 0
CUI: C1846169
Disease: Myotubular Myopathy with Abnormal Genital Development
Myotubular Myopathy with Abnormal Genital Development 		2 0 1 0.14 0 0
CUI: C1846175
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder) 		2 0 1 0.14 0 0
CUI: C1850627
Disease: Nasodigitoacoustic syndrome
Nasodigitoacoustic syndrome 		2 0 1 0.14 0 0