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: C1861355
Disease: Syndactyly, Type IV
Syndactyly, Type IV 		3 0 1 0.17 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals 		3 0 1 0.17 0 0
CUI: C1864827
Disease: HOLOPROSENCEPHALY 5
HOLOPROSENCEPHALY 5 		3 0 1 0.17 0 0
CUI: C4021638
Disease: Absent nasal septal cartilage
Absent nasal septal cartilage 		3 0 1 0.17 0 0
CUI: C4023728
Disease: 1-5 finger syndactyly
1-5 finger syndactyly 		3 0 1 0.17 0 0
CUI: C4082761
Disease: Abnormality of limb bone morphology
Abnormality of limb bone morphology 		3 0 1 0.17 0 0
CUI: C0014013
Disease: Empyema, Pleural
Empyema, Pleural 		4 0 1 0.14 0 0
CUI: C1868114
Disease: POLYDACTYLY, PREAXIAL II (disorder)
POLYDACTYLY, PREAXIAL II (disorder) 		4 0 1 0.14 0 0
CUI: C3711749
Disease: Nonsyndromic Holoprosencephaly
Nonsyndromic Holoprosencephaly 		4 0 1 0.14 0 0
CUI: C3897042
Disease: Smoldering Systemic Mastocytosis
Smoldering Systemic Mastocytosis 		4 0 1 0.14 0 0
CUI: C4330667
Disease: Medulloblastoma, Non-WNT/Non-SHH
Medulloblastoma, Non-WNT/Non-SHH 		4 0 1 0.14 0 0
CUI: C0032026
Disease: Pityriasis Rosea
Pityriasis Rosea 		5 0 1 0.12 0 0
CUI: C0239182
Disease: Watery diarrhoea
Watery diarrhoea 		5 0 1 0.12 0 0
CUI: C0423063
Disease: Comitant heterophoria
Comitant heterophoria 		5 0 1 0.12 0 0
CUI: C0685682
Disease: Single naris
Single naris 		5 0 1 0.12 0 0
CUI: C1838610
Disease: Aplasia of the 1st metacarpal
Aplasia of the 1st metacarpal 		5 0 1 0.12 0 0
CUI: C1881600
Disease: Malignant Vipoma
Malignant Vipoma 		5 0 1 0.12 0 0
CUI: C4021100
Disease: Increased fibular diameter
Increased fibular diameter 		5 0 1 0.12 0 0
CUI: C0011993
Disease: Vipoma
Vipoma 		6 0 1 0.11 0 0
CUI: C0016325
Disease: Fluoride Poisoning
Fluoride Poisoning 		6 0 1 0.11 0 0
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		16 0 2 0.11 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 2 0.11 0 0
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		17 0 2 0.11 0 0
CUI: C0265633
Disease: Congenital absence of tibia
Congenital absence of tibia 		7 0 1 1.0E-01 0 0
CUI: C0403766
Disease: Acquired phimosis
Acquired phimosis 		7 0 1 1.0E-01 0 0