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: C1857941
Disease: Brooke-Spiegler syndrome
Brooke-Spiegler syndrome 		45 0 23 0.36 0 0
CUI: C0036992
Disease: Short Bowel Syndrome
Short Bowel Syndrome 		21 0 12 0.24 0 0
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia 		34 31 10 0.15 2 4.8E-02
CUI: C0340978
Disease: May-Hegglin anomaly
May-Hegglin anomaly 		12 19 7 0.15 11 0.52
CUI: C0005129
Disease: Bernard-Soulier Syndrome
Bernard-Soulier Syndrome 		46 0 10 0.13 0 0
CUI: C4281802
Disease: Spongiform encephalopathy
Spongiform encephalopathy 		14 0 6 0.12 0 0
CUI: C0542141
Disease: Paralysis radial
Paralysis radial 		5 0 5 0.12 0 0
CUI: C1306600
Disease: Radial nerve palsy
Radial nerve palsy 		5 0 5 0.12 0 0
CUI: C3854629
Disease: Tendon thickening
Tendon thickening 		6 0 5 0.12 0 0
CUI: C0263374
Disease: Lichen striatus
Lichen striatus 		7 0 5 0.11 0 0
CUI: C0398642
Disease: Montreal platelet syndrome
Montreal platelet syndrome 		7 0 5 0.11 0 0
CUI: C0036457
Disease: Scrapie
Scrapie 		8 0 5 0.11 0 0
CUI: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		9 0 5 0.11 0 0
CUI: C0861727
Disease: Pancreatic adenocarcinoma metastatic
Pancreatic adenocarcinoma metastatic 		32 0 7 0.10 0 0
CUI: C0028841
Disease: Ocular Hypotension
Ocular Hypotension 		22 0 6 0.10 0 0
CUI: C4728082
Disease: Severe hypoglycaemia
Severe hypoglycaemia 		36 0 7 9.9E-02 0 0
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia 		25 0 6 9.8E-02 0 0
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders 		59 0 9 9.8E-02 0 0
CUI: C0016807
Disease: Functional disorder of intestine
Functional disorder of intestine 		4 0 4 9.5E-02 0 0
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time 		39 0 7 9.5E-02 0 0
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation 		16 0 5 9.4E-02 0 0
CUI: C4310512
Disease: Sporadic CJD
Sporadic CJD 		30 0 6 9.1E-02 0 0
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		19 0 5 8.9E-02 0 0
CUI: C0032027
Disease: Pityriasis Rubra Pilaris
Pityriasis Rubra Pilaris 		32 0 6 8.8E-02 0 0
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode 		8 0 4 8.7E-02 0 0