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: C0850826
Disease: Localized skin lesion
Localized skin lesion 		2 0 1 0.33 0 0
CUI: C1419610
Disease: RP23 gene
RP23 gene 		2 0 1 0.33 0 0
CUI: C1835574
Disease: Bipartite calcaneus
Bipartite calcaneus 		2 0 1 0.33 0 0
CUI: C1839507
Disease: Thick skull base
Thick skull base 		2 0 1 0.33 0 0
CUI: C1839512
Disease: Limited knee flexion
Limited knee flexion 		2 0 1 0.33 0 0
CUI: C1839822
Disease: Anterior concavity of thoracic vertebrae
Anterior concavity of thoracic vertebrae 		2 0 1 0.33 0 0
CUI: C1839830
Disease: Frontal hirsutism
Frontal hirsutism 		2 0 1 0.33 0 0
CUI: C1844512
Disease: Anteriorly placed odontoid process
Anteriorly placed odontoid process 		2 0 1 0.33 0 0
CUI: C1844696
Disease: OTOPALATODIGITAL SYNDROME, TYPE II
OTOPALATODIGITAL SYNDROME, TYPE II 		2 21 1 0.33 1 4.2E-02
CUI: C1844706
Disease: Rudimentary fibula
Rudimentary fibula 		2 0 1 0.33 0 0
CUI: C1846175
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder) 		2 0 1 0.33 0 0
CUI: C1850631
Disease: Short 3rd metacarpal
Short 3rd metacarpal 		2 0 1 0.33 0 0
CUI: C1858545
Disease: Facial capillary hemangioma
Facial capillary hemangioma 		2 0 1 0.33 0 0
CUI: C2931426
Disease: Orofaciodigital syndrome type1
Orofaciodigital syndrome type1 		2 0 1 0.33 0 0
CUI: C4021244
Disease: Abnormal hand bone ossification
Abnormal hand bone ossification 		2 0 1 0.33 0 0
CUI: C4021335
Disease: Short distal phalanx of hallux
Short distal phalanx of hallux 		2 0 1 0.33 0 0
CUI: C4022002
Disease: Thoracoabdominal wall defect
Thoracoabdominal wall defect 		2 0 1 0.33 0 0
CUI: C4025010
Disease: Coat hanger sign of ribs
Coat hanger sign of ribs 		2 0 1 0.33 0 0
CUI: C4025086
Disease: Irregular metacarpals
Irregular metacarpals 		2 0 1 0.33 0 0
CUI: C4025747
Disease: Bulbous tips of toes
Bulbous tips of toes 		2 0 1 0.33 0 0
CUI: C4280644
Disease: Increased size of the mandible
Increased size of the mandible 		2 0 1 0.33 0 0
CUI: C1839965
Disease: Multiple impacted teeth
Multiple impacted teeth 		3 0 1 0.25 0 0
CUI: C1844509
Disease: Antegonial notching of mandible
Antegonial notching of mandible 		3 0 1 0.25 0 0
CUI: C1845546
Disease: FG SYNDROME 4 (disorder)
FG SYNDROME 4 (disorder) 		3 0 1 0.25 0 0
CUI: C1845567
Disease: FG SYNDROME 3
FG SYNDROME 3 		3 0 1 0.25 0 0