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: C1849293
Disease: Advanced tarsal ossification
Advanced tarsal ossification 		4 0 2 0.25 0 0
CUI: C1850293
Disease: Severe platyspondyly
Severe platyspondyly 		5 0 2 0.22 0 0
CUI: C1837082
Disease: Metaphyseal cupping
Metaphyseal cupping 		13 0 3 0.19 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 0.17 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 0.17 0 0
CUI: C0432219
Disease: Opsismodysplasia
Opsismodysplasia 		1 0 1 0.17 0 0
CUI: C1834993
Disease: Prominent supraorbital arches in adult
Prominent supraorbital arches in adult 		1 0 1 0.17 0 0
CUI: C1838779
Disease: Eiken Skeletal Dysplasia
Eiken Skeletal Dysplasia 		1 0 1 0.17 0 0
CUI: C4225378
Disease: SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY 		1 0 1 0.17 0 0
CUI: C4540355
Disease: JOUBERT SYNDROME 31
JOUBERT SYNDROME 31 		1 0 1 0.17 0 0
CUI: C4693870
Disease: EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2
EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2 		1 0 1 0.17 0 0
CUI: C0432194
Disease: Schneckenbecken dysplasia
Schneckenbecken dysplasia 		2 0 1 0.14 0 0
CUI: C0597647
Disease: viral leukemogenesis
viral leukemogenesis 		2 0 1 0.14 0 0
CUI: C1290587
Disease: Failure of tooth eruption
Failure of tooth eruption 		2 0 1 0.14 0 0
CUI: C1839507
Disease: Thick skull base
Thick skull base 		2 0 1 0.14 0 0
CUI: C1859158
Disease: Laryngeal calcification
Laryngeal calcification 		2 0 1 0.14 0 0
CUI: C1969092
Disease: NEPHRONOPHTHISIS 7
NEPHRONOPHTHISIS 7 		2 0 1 0.14 0 0
CUI: C2750075
Disease: Chondrodysplasia, Megarbane-Dagher-Melki Type
Chondrodysplasia, Megarbane-Dagher-Melki Type 		2 0 1 0.14 0 0
CUI: C4021862
Disease: Absent epiphyses
Absent epiphyses 		2 0 1 0.14 0 0
CUI: C0272214
Disease: Persistent lymphocytosis
Persistent lymphocytosis 		3 0 1 0.12 0 0
CUI: C0424693
Disease: Broad skull
Broad skull 		3 0 1 0.12 0 0
CUI: C0431414
Disease: Sacral dysgenesis
Sacral dysgenesis 		3 0 1 0.12 0 0
CUI: C0795910
Disease: COWCHOCK SYNDROME
COWCHOCK SYNDROME 		3 0 1 0.12 0 0
CUI: C1839413
Disease: Pyruvate Dehydrogenase E1 Alpha Deficiency
Pyruvate Dehydrogenase E1 Alpha Deficiency 		3 0 1 0.12 0 0
CUI: C1856922
Disease: Limited elbow flexion
Limited elbow flexion 		3 0 1 0.12 0 0