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: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		0 1 0 0 1 0.20
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		0 1 0 0 1 0.20
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis 		0 24 0 0 1 3.6E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 0.20
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 1 1 7.1E-02 1 0.20
CUI: C0006897
Disease: Capillariasis
Capillariasis 		1 0 1 7.1E-02 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis 		1 0 1 7.1E-02 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness 		1 0 1 7.1E-02 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection 		1 0 1 7.1E-02 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 7.1E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 7.1E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 7.1E-02 0 0
CUI: C0262568
Disease: Subendocardial myocardial infarction
Subendocardial myocardial infarction 		1 0 1 7.1E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 7.1E-02 0 0
CUI: C0332561
Disease: Fibrous nodule
Fibrous nodule 		1 0 1 7.1E-02 0 0
CUI: C0751505
Disease: Insufficient Sleep Syndrome
Insufficient Sleep Syndrome 		1 0 1 7.1E-02 0 0
CUI: C0751507
Disease: Sleep Fragmentation
Sleep Fragmentation 		1 0 1 7.1E-02 0 0
CUI: C1262200
Disease: Cerebrovascular infarction
Cerebrovascular infarction 		1 0 1 7.1E-02 0 0
CUI: C1265787
Disease: Single cyst
Single cyst 		1 0 1 7.1E-02 0 0
CUI: C1328061
Disease: Myelodysplastic/myeloproliferative neoplasm, unclassifiable
Myelodysplastic/myeloproliferative neoplasm, unclassifiable 		1 1 1 7.1E-02 1 0.20
CUI: C1456542
Disease: Genetic Brain Disorders
Genetic Brain Disorders 		1 0 1 7.1E-02 0 0
CUI: C1516553
Disease: Prefibrotic/Early Primary Myelofibrosis
Prefibrotic/Early Primary Myelofibrosis 		1 1 1 7.1E-02 1 0.20
CUI: C1565106
Disease: Headache Disorders, Primary
Headache Disorders, Primary 		1 0 1 7.1E-02 0 0
CUI: C1851184
Disease: Fibrinolytic Defect
Fibrinolytic Defect 		1 0 1 7.1E-02 0 0
CUI: C2675105
Disease: BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC 		1 1 1 7.1E-02 1 0.20