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: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		5 0 4 0.25 0 0
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		5 0 4 0.25 0 0
CUI: C0431863
Disease: Carpal synostosis
Carpal synostosis 		15 0 5 0.20 0 0
CUI: C1862313
Disease: Short distal phalanx of the thumb
Short distal phalanx of the thumb 		7 0 3 0.16 0 0
CUI: C1836186
Disease: Fibular aplasia
Fibular aplasia 		9 0 3 0.14 0 0
CUI: C0265609
Disease: Accessory carpal bones
Accessory carpal bones 		2 0 2 0.13 0 0
CUI: C1835574
Disease: Bipartite calcaneus
Bipartite calcaneus 		2 0 2 0.13 0 0
CUI: C1849575
Disease: Absence of labia majora
Absence of labia majora 		2 0 2 0.13 0 0
CUI: C4021073
Disease: Morphological abnormality of the gastrointestinal tract
Morphological abnormality of the gastrointestinal tract 		2 0 2 0.13 0 0
CUI: C4021335
Disease: Short distal phalanx of hallux
Short distal phalanx of hallux 		2 0 2 0.13 0 0
CUI: C4025086
Disease: Irregular metacarpals
Irregular metacarpals 		2 0 2 0.13 0 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		12 5 3 0.12 2 0.40
CUI: C1856780
Disease: Posterior vertebral hypoplasia
Posterior vertebral hypoplasia 		3 0 2 0.12 0 0
CUI: C1867439
Disease: Pterygium, Antecubital
Pterygium, Antecubital 		3 0 2 0.12 0 0
CUI: C0265654
Disease: Tarsal Coalition
Tarsal Coalition 		22 0 4 0.12 0 0
CUI: C0265293
Disease: Frontometaphyseal dysplasia
Frontometaphyseal dysplasia 		4 0 2 0.12 0 0
CUI: C1867448
Disease: Multiple pterygia
Multiple pterygia 		4 0 2 0.12 0 0
CUI: C3151523
Disease: Abnormal cervical curvature
Abnormal cervical curvature 		4 0 2 0.12 0 0
CUI: C4021260
Disease: Long metacarpals
Long metacarpals 		4 0 2 0.12 0 0
CUI: C4025056
Disease: Failure of eruption of permanent teeth
Failure of eruption of permanent teeth 		5 0 2 0.11 0 0
CUI: C0240414
Disease: Hypoplasia of muscle
Hypoplasia of muscle 		6 0 2 0.11 0 0
CUI: C1856639
Disease: Absent/hypoplastic paranasal sinuses
Absent/hypoplastic paranasal sinuses 		6 0 2 0.11 0 0
CUI: C1861689
Disease: KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT
KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT 		6 0 2 0.11 0 0
CUI: C1865571
Disease: Aplasia/Hypoplasia of the ulna
Aplasia/Hypoplasia of the ulna 		6 0 2 0.11 0 0
CUI: C3805420
Disease: Popliteal pterygium
Popliteal pterygium 		6 0 2 0.11 0 0