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: C1840062
Disease: Hypoplasia of the lesser trochanter
Hypoplasia of the lesser trochanter 		1 0 1 1.00 0 0
CUI: C1868581
Disease: Patella aplasia, coxa vara, tarsal synostosis
Patella aplasia, coxa vara, tarsal synostosis 		1 0 1 1.00 0 0
CUI: C3150607
Disease: CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME
CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME 		1 0 1 1.00 0 0
CUI: C3150880
Disease: CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME
CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME 		1 0 1 1.00 0 0
CUI: C4024622
Disease: Wide capital femoral epiphyses
Wide capital femoral epiphyses 		1 0 1 1.00 0 0
CUI: C4025155
Disease: Talocalcaneal synostosis
Talocalcaneal synostosis 		1 0 1 1.00 0 0
CUI: C0002447
Disease: Amelia
Amelia 		2 0 1 0.50 0 0
CUI: C1860826
Disease: Coxa Magna
Coxa Magna 		2 0 1 0.50 0 0
CUI: C3872820
Disease: Congenital pulmonary acinar dysplasia
Congenital pulmonary acinar dysplasia 		2 0 1 0.50 0 0
CUI: C1853566
Disease: Genitopatellar Syndrome
Genitopatellar Syndrome 		3 0 1 0.33 0 0
CUI: C1840068
Disease: Patellar hypoplasia
Patellar hypoplasia 		5 0 1 0.20 0 0
CUI: C3697119
Disease: Pulmonary arterial hypertension associated with congenital heart disease
Pulmonary arterial hypertension associated with congenital heart disease 		5 0 1 0.20 0 0
CUI: C0521648
Disease: Neonatal respiratory failure
Neonatal respiratory failure 		8 0 1 0.12 0 0
CUI: C1854910
Disease: Shallow acetabular fossae
Shallow acetabular fossae 		8 0 1 0.12 0 0
CUI: C3887658
Disease: PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT
PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT 		8 0 1 0.12 0 0
CUI: C0221363
Disease: Bifid nose
Bifid nose 		9 0 1 0.11 0 0
CUI: C1696701
Disease: Skin-picking
Skin-picking 		10 0 1 1.0E-01 0 0
CUI: C1842155
Disease: Flat capital femoral epiphysis
Flat capital femoral epiphysis 		11 0 1 9.1E-02 0 0
CUI: C1701939
Disease: Familial pulmonary arterial hypertension
Familial pulmonary arterial hypertension 		12 0 1 8.3E-02 0 0
CUI: C1150929
Disease: 2-oxo-hept-3-ene-1,7-dioate hydratase activity
2-oxo-hept-3-ene-1,7-dioate hydratase activity 		14 0 1 7.1E-02 0 0
CUI: C1868578
Disease: Patellar aplasia
Patellar aplasia 		17 0 1 5.9E-02 0 0
CUI: C1858539
Disease: Shawl scrotum
Shawl scrotum 		19 0 1 5.3E-02 0 0
CUI: C1868577
Disease: Patella aplasia-hypoplasia
Patella aplasia-hypoplasia 		20 0 1 5.0E-02 0 0
CUI: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME 		21 0 1 4.8E-02 0 0
CUI: C0345375
Disease: Congenital hypoplasia of femur
Congenital hypoplasia of femur 		22 0 1 4.5E-02 0 0