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: C0014854
Disease: Esophageal diverticulum
Esophageal diverticulum 		1 0 1 7.1E-02 0 0
CUI: C0432219
Disease: Opsismodysplasia
Opsismodysplasia 		1 0 1 7.1E-02 0 0
CUI: C1849290
Disease: Snail-like ilia
Snail-like ilia 		1 0 1 7.1E-02 0 0
CUI: C1855000
Disease: Agenesis of central incisor
Agenesis of central incisor 		1 0 1 7.1E-02 0 0
CUI: C2931889
Disease: Oral-facial-digital syndrome, type 2
Oral-facial-digital syndrome, type 2 		1 0 1 7.1E-02 0 0
CUI: C3151120
Disease: MEIER-GORLIN SYNDROME 4
MEIER-GORLIN SYNDROME 4 		1 0 1 7.1E-02 0 0
CUI: C3806516
Disease: Disproportionate shortening of the tibia
Disproportionate shortening of the tibia 		1 0 1 7.1E-02 0 0
CUI: C3809691
Disease: SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY 		1 0 1 7.1E-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 7.1E-02 0 0
CUI: C4017085
Disease: SHORT-RIB THORACIC DYSPLASIA 10 WITH POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 10 WITH POLYDACTYLY 		1 0 1 7.1E-02 0 0
CUI: C4021336
Disease: Complete duplication of hallux phalanx
Complete duplication of hallux phalanx 		1 0 1 7.1E-02 0 0
CUI: C4021589
Disease: Absent glenoid fossa
Absent glenoid fossa 		1 0 1 7.1E-02 0 0
CUI: C4021618
Disease: Polysyndactyly of hallux
Polysyndactyly of hallux 		1 0 1 7.1E-02 0 0
CUI: C4024675
Disease: C1-C2 vertebral abnormality
C1-C2 vertebral abnormality 		1 0 1 7.1E-02 0 0
CUI: C4477070
Disease: Unilateral alveolar cleft of maxilla
Unilateral alveolar cleft of maxilla 		1 0 1 7.1E-02 0 0
CUI: C4479416
Disease: SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY 		1 0 1 7.1E-02 0 0
CUI: C4552001
Disease: MEIER-GORLIN SYNDROME 1
MEIER-GORLIN SYNDROME 1 		1 0 1 7.1E-02 0 0
CUI: C4693523
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24 		1 0 1 7.1E-02 0 0
CUI: C4693524
Disease: SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY 		1 0 1 7.1E-02 0 0
CUI: C4693616
Disease: SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY 		1 0 1 7.1E-02 0 0
CUI: C4693640
Disease: OROFACIODIGITAL SYNDROME XVII
OROFACIODIGITAL SYNDROME XVII 		1 0 1 7.1E-02 0 0
CUI: C4694006
Disease: SHORT-RIB THORACIC DYSPLASIA 19 WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 19 WITHOUT POLYDACTYLY 		1 0 1 7.1E-02 0 0
CUI: C4694024
Disease: SHORT-RIB THORACIC DYSPLASIA 20/7 WITH POLYDACTYLY, DIGENIC (1 patient)
SHORT-RIB THORACIC DYSPLASIA 20/7 WITH POLYDACTYLY, DIGENIC (1 patient) 		1 0 1 7.1E-02 0 0
CUI: C0238591
Disease: Adactyly
Adactyly 		2 0 1 6.7E-02 0 0
CUI: C0266317
Disease: Megacalycosis
Megacalycosis 		2 0 1 6.7E-02 0 0