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: C0024215
Disease: Lymphangiectasis, Intestinal
Lymphangiectasis, Intestinal 		0 1 0 0 1 1.5E-02
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		0 1 0 0 1 1.5E-02
CUI: C3809356
Disease: MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3
MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3 		0 11 0 0 1 1.3E-02
CUI: C4014660
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20 		0 6 0 0 1 1.4E-02
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 1.5E-03 0 0
CUI: C0019079
Disease: Hemoptysis
Hemoptysis 		67 0 1 1.5E-03 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 1.6E-03 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 1.6E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 1.6E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.6E-03 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		57 0 1 1.6E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 1.6E-03 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 1 1.6E-03 0 0
CUI: C0403824
Disease: Teratozoospermia
Teratozoospermia 		53 0 1 1.6E-03 0 0
CUI: C0020672
Disease: Hypothermia, natural
Hypothermia, natural 		52 0 1 1.6E-03 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 1 1.6E-03 0 0
CUI: C1334968
Disease: Nodular Lymphocyte Predominant Hodgkin Lymphoma
Nodular Lymphocyte Predominant Hodgkin Lymphoma 		51 0 1 1.6E-03 0 0
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 0 1 1.6E-03 0 0
CUI: C4699152
Disease: ST-segment elevation myocardial infarction (STEMI)
ST-segment elevation myocardial infarction (STEMI) 		51 0 1 1.6E-03 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 1.6E-03 0 0
CUI: C0239138
Disease: Hip joint varus deformity - observation
Hip joint varus deformity - observation 		49 0 1 1.6E-03 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 1 1.6E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.6E-03 0 0
CUI: C0023794
Disease: Lipoidosis
Lipoidosis 		44 0 1 1.6E-03 0 0
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		44 0 1 1.6E-03 0 0