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: C1839798
Disease: Long nose
Long nose 		29 0 7 0.18 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx 		10 0 3 0.12 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin 		2 0 2 0.12 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal 		2 0 2 0.12 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 2 0.12 0 0
CUI: C4021360
Disease: Partial duplication of the distal phalanx of the 3rd finger
Partial duplication of the distal phalanx of the 3rd finger 		2 0 2 0.12 0 0
CUI: C4021365
Disease: Partial duplication of the distal phalanx of the 2nd finger
Partial duplication of the distal phalanx of the 2nd finger 		2 0 2 0.12 0 0
CUI: C1510455
Disease: Acrocephalosyndactylia
Acrocephalosyndactylia 		3 0 2 0.11 0 0
CUI: C4021377
Disease: Prominent crus of helix
Prominent crus of helix 		3 0 2 0.11 0 0
CUI: C0432090
Disease: Cleft of hard palate
Cleft of hard palate 		4 0 2 0.11 0 0
CUI: C0546297
Disease: Hallux Varus
Hallux Varus 		4 0 2 0.11 0 0
CUI: C1858569
Disease: Absence of Stensen duct
Absence of Stensen duct 		4 0 2 0.11 0 0
CUI: C4025596
Disease: Abnormality of connective tissue
Abnormality of connective tissue 		4 0 2 0.11 0 0
CUI: C0003614
Disease: Appendiceal Neoplasms
Appendiceal Neoplasms 		5 0 2 1.0E-01 0 0
CUI: C0265269
Disease: Lacrimoauriculodentodigital syndrome
Lacrimoauriculodentodigital syndrome 		5 0 2 1.0E-01 0 0
CUI: C0266184
Disease: Congenital duodenal obstruction due to malrotation of intestine
Congenital duodenal obstruction due to malrotation of intestine 		5 0 2 1.0E-01 0 0
CUI: C0424690
Disease: Asymmetrical skull
Asymmetrical skull 		5 0 2 1.0E-01 0 0
CUI: C1708747
Disease: Low grade appendiceal mucinous neoplasm
Low grade appendiceal mucinous neoplasm 		5 0 2 1.0E-01 0 0
CUI: C2676443
Disease: Proximal radio-ulnar synostosis
Proximal radio-ulnar synostosis 		5 0 2 1.0E-01 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 3 9.7E-02 0 0
CUI: C1857456
Disease: Morphological abnormality of the middle ear
Morphological abnormality of the middle ear 		6 0 2 9.5E-02 0 0
CUI: C1867060
Disease: Lacrimal Puncta, Absence of
Lacrimal Puncta, Absence of 		6 0 2 9.5E-02 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 2 9.5E-02 0 0
CUI: C4024618
Disease: Large iliac wings
Large iliac wings 		6 0 2 9.5E-02 0 0
CUI: C1842231
Disease: Broad metatarsal
Broad metatarsal 		7 0 2 9.1E-02 0 0