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: C0334569
Disease: Odontogenic myxoma
Odontogenic myxoma 		8 0 3 0.12 0 0
CUI: C1859363
Disease: Abnormality of dental eruption
Abnormality of dental eruption 		10 1 3 0.12 1 1.00
CUI: C2032780
Disease: Palate fistula
Palate fistula 		10 1 3 0.12 1 1.00
CUI: C0392519
Disease: Calcium deficiency
Calcium deficiency 		2 0 2 0.11 0 0
CUI: C1306839
Disease: Pyrophosphate arthritis
Pyrophosphate arthritis 		2 0 2 0.11 0 0
CUI: C1835583
Disease: Multiple long-bone exostoses
Multiple long-bone exostoses 		2 0 2 0.11 0 0
CUI: C2014414
Disease: orthopedic disorders
orthopedic disorders 		2 0 2 0.11 0 0
CUI: C4021377
Disease: Prominent crus of helix
Prominent crus of helix 		3 0 2 1.0E-01 0 0
CUI: C4025078
Disease: Tapering pointed ends of distal finger phalanges
Tapering pointed ends of distal finger phalanges 		4 0 2 9.5E-02 0 0
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome 		4 0 2 9.5E-02 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		17 0 3 9.1E-02 0 0
CUI: C0546952
Disease: Congenital facial asymmetry
Congenital facial asymmetry 		5 0 2 9.1E-02 0 0
CUI: C0685775
Disease: Congenital absence of jaw
Congenital absence of jaw 		5 0 2 9.1E-02 0 0
CUI: C0846967
Disease: Acanthoma
Acanthoma 		5 0 2 9.1E-02 0 0
CUI: C2676443
Disease: Proximal radio-ulnar synostosis
Proximal radio-ulnar synostosis 		5 0 2 9.1E-02 0 0
CUI: C4023418
Disease: Unicoronal synostosis
Unicoronal synostosis 		5 0 2 9.1E-02 0 0
CUI: C0265255
Disease: Trichorhinophalangeal syndrome
Trichorhinophalangeal syndrome 		6 0 2 8.7E-02 0 0
CUI: C1846438
Disease: Hypoplastic facial bones
Hypoplastic facial bones 		6 1 2 8.7E-02 1 1.00
CUI: C3553517
Disease: CORNELIA DE LANGE SYNDROME 4
CORNELIA DE LANGE SYNDROME 4 		6 0 2 8.7E-02 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 2 8.7E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 3 8.3E-02 0 0
CUI: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy 		7 0 2 8.3E-02 0 0
CUI: C0334265
Disease: Transitional Cell Neoplasm
Transitional Cell Neoplasm 		7 0 2 8.3E-02 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		8 0 2 8.0E-02 0 0
CUI: C0241703
Disease: High pitched voice
High pitched voice 		35 0 4 8.0E-02 0 0