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: C0233737
Disease: Circumlocution
Circumlocution 		1 0 1 3.4E-02 0 0
CUI: C0264491
Disease: Acute-on-chronic respiratory failure
Acute-on-chronic respiratory failure 		1 0 1 3.4E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 3.4E-02 0 0
CUI: C0406707
Disease: Basan syndrome
Basan syndrome 		1 0 1 3.4E-02 0 0
CUI: C0478093
Disease: Other congenital malformation syndromes with other skeletal changes
Other congenital malformation syndromes with other skeletal changes 		1 0 1 3.4E-02 0 0
CUI: C0740850
Disease: airway disease restrictive
airway disease restrictive 		1 0 1 3.4E-02 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 3.4E-02 0 0
CUI: C1836916
Disease: POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA 		1 0 1 3.4E-02 0 0
CUI: C1837464
Disease: Small eyes
Small eyes 		1 0 1 3.4E-02 0 0
CUI: C1837481
Disease: Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related 		1 0 1 3.4E-02 0 0
CUI: C1837487
Disease: Dysplastic iliac wings
Dysplastic iliac wings 		1 0 1 3.4E-02 0 0
CUI: C1859120
Disease: Anterior rib punctate calcifications
Anterior rib punctate calcifications 		1 0 1 3.4E-02 0 0
CUI: C1859121
Disease: Sternal punctate calcifications
Sternal punctate calcifications 		1 0 1 3.4E-02 0 0
CUI: C1866048
Disease: Severe hydrops fetalis
Severe hydrops fetalis 		1 0 1 3.4E-02 0 0
CUI: C1970005
Disease: Asphyxiating Thoracic Dystrophy 2
Asphyxiating Thoracic Dystrophy 2 		1 5 1 3.4E-02 1 8.3E-03
CUI: C3179244
Disease: Pseudo Pelger-Huet Anomaly
Pseudo Pelger-Huet Anomaly 		1 0 1 3.4E-02 0 0
CUI: C3279792
Disease: SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY 		1 13 1 3.4E-02 2 1.6E-02
CUI: C3280598
Disease: SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY 		1 5 1 3.4E-02 1 8.3E-03
CUI: C3280612
Disease: NEPHRONOPHTHISIS 13
NEPHRONOPHTHISIS 13 		1 6 1 3.4E-02 1 8.3E-03
CUI: C3809691
Disease: SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY 		1 0 1 3.4E-02 0 0
CUI: C3810200
Disease: SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY 		1 0 1 3.4E-02 0 0
CUI: C3887526
Disease: OSTEOARTHRITIS SUSCEPTIBILITY 2
OSTEOARTHRITIS SUSCEPTIBILITY 2 		1 0 1 3.4E-02 0 0
CUI: C4017085
Disease: SHORT-RIB THORACIC DYSPLASIA 10 WITH POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 10 WITH POLYDACTYLY 		1 0 1 3.4E-02 0 0
CUI: C4017372
Disease: SHORT-RIB THORACIC DYSPLASIA WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA WITHOUT POLYDACTYLY 		1 0 1 3.4E-02 0 0
CUI: C4021245
Disease: Patchy variation in bone mineral density
Patchy variation in bone mineral density 		1 0 1 3.4E-02 0 0