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: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 5 0.16 0 0
CUI: C1389280
Disease: Basal ganglia calcification
Basal ganglia calcification 		22 0 4 0.16 0 0
CUI: C2981140
Disease: Glaucoma of childhood
Glaucoma of childhood 		30 0 5 0.16 0 0
CUI: C0272263
Disease: Cryofibrinogenemia
Cryofibrinogenemia 		1 0 1 0.14 0 0
CUI: C0393968
Disease: Systemic lupus erythematosus encephalitis
Systemic lupus erythematosus encephalitis 		1 0 1 0.14 0 0
CUI: C0456097
Disease: Congenital viral disease
Congenital viral disease 		1 0 1 0.14 0 0
CUI: C0477365
Disease: Other specified degenerative diseases of nervous system
Other specified degenerative diseases of nervous system 		1 0 1 0.14 0 0
CUI: C0751740
Disease: Lenticulostriate Vasculopathy
Lenticulostriate Vasculopathy 		1 0 1 0.14 0 0
CUI: C1969286
Disease: Hypoplastic distal radial epiphyses
Hypoplastic distal radial epiphyses 		1 0 1 0.14 0 0
CUI: C1969287
Disease: Expanded phalanges with widened medullary cavities
Expanded phalanges with widened medullary cavities 		1 0 1 0.14 0 0
CUI: C1969288
Disease: Expanded metacarpals with widened medullary cavities
Expanded metacarpals with widened medullary cavities 		1 0 1 0.14 0 0
CUI: C1969289
Disease: Expanded metatarsals with widened medullary cavities
Expanded metatarsals with widened medullary cavities 		1 0 1 0.14 0 0
CUI: C1969291
Disease: Aortic arch calcification
Aortic arch calcification 		1 0 1 0.14 0 0
CUI: C3277693
Disease: Punctate vasculitis skin lesions
Punctate vasculitis skin lesions 		1 0 1 0.14 0 0
CUI: C3280721
Disease: CHILBLAIN LUPUS 2
CHILBLAIN LUPUS 2 		1 0 1 0.14 0 0
CUI: C4025055
Disease: Hypoplasia of the tooth germ
Hypoplasia of the tooth germ 		1 0 1 0.14 0 0
CUI: C4303564
Disease: Hereditary vascular retinopathy
Hereditary vascular retinopathy 		1 0 1 0.14 0 0
CUI: C4303791
Disease: Cerebroretinal vasculopathy
Cerebroretinal vasculopathy 		1 0 1 0.14 0 0
CUI: C4479376
Disease: PSEUDO-TORCH SYNDROME 2
PSEUDO-TORCH SYNDROME 2 		1 0 1 0.14 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		34 0 5 0.14 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 5 0.14 0 0
CUI: C0030326
Disease: Panniculitis
Panniculitis 		37 0 5 0.13 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech 		37 0 5 0.13 0 0
CUI: C0025062
Disease: Mediastinal Emphysema
Mediastinal Emphysema 		2 0 1 0.12 0 0
CUI: C0271899
Disease: Normocytic normochromic anemia
Normocytic normochromic anemia 		2 1 1 0.12 1 3.8E-02