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: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 9 0.12 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia 		63 0 11 0.12 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 9 0.12 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts 		46 0 9 0.12 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		46 0 9 0.12 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		30 0 7 0.11 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 10 0.11 0 0
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia 		67 0 10 0.10 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism 		92 0 12 1.0E-01 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 5 1.0E-01 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		60 0 9 9.9E-02 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis 		62 0 9 9.7E-02 0 0
CUI: C1276035
Disease: Pena-Shokeir syndrome type I
Pena-Shokeir syndrome type I 		40 0 7 9.6E-02 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 10 9.5E-02 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 4 9.3E-02 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 4 9.3E-02 0 0
CUI: C0034150
Disease: Purpura
Purpura 		68 0 9 9.1E-02 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 11 9.0E-02 0 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		70 0 9 8.9E-02 0 0
CUI: C2732374
Disease: Edema of dorsum of hand
Edema of dorsum of hand 		9 0 4 8.9E-02 0 0
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin 		50 0 7 8.4E-02 0 0
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		76 0 9 8.4E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		102 0 11 8.4E-02 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		77 0 9 8.3E-02 0 0
CUI: C1848873
Disease: Abnormality of the diaphragm
Abnormality of the diaphragm 		12 0 4 8.3E-02 0 0