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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 6.7E-02
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		0 119 0 0 1 8.0E-03
CUI: C0021845
Disease: Intestinal Perforation
Intestinal Perforation 		0 3 0 0 1 0.11
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		0 2 0 0 1 0.12
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.14
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0 9 0 0 1 6.7E-02
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder 		0 9 0 0 1 6.7E-02
CUI: C0496779
Disease: Malignant neoplasm of appendix
Malignant neoplasm of appendix 		0 2 0 0 1 0.12
CUI: C0796003
Disease: Juberg-Marsidi syndrome
Juberg-Marsidi syndrome 		0 14 0 0 1 5.0E-02
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		0 82 0 0 1 1.1E-02
CUI: C1306050
Disease: Primary malignant neoplasm of appendix
Primary malignant neoplasm of appendix 		0 2 0 0 1 0.12
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 1 3.7E-02
CUI: C1720430
Disease: Papillary carcinoma, clear cell
Papillary carcinoma, clear cell 		0 2 0 0 1 0.12
CUI: C1842408
Disease: increased risk of pancreatic cancer
increased risk of pancreatic cancer 		0 6 0 0 1 8.3E-02
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		0 14 0 0 1 5.0E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 0.11
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft 		0 2 0 0 1 0.12
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis 		0 36 0 0 1 2.4E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.14
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 6.2E-02
CUI: C3854181
Disease: Nevus sebaceous
Nevus sebaceous 		0 4 0 0 1 1.0E-01
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.14
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 0.12
CUI: C4302356
Disease: Primary low grade serous adenocarcinoma of ovary
Primary low grade serous adenocarcinoma of ovary 		0 1 0 0 1 0.14
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
Nevus Sebaceus of Jadassohn 		0 7 0 0 1 7.7E-02