Source: CURATED ×
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: C0432416
Disease: Down Syndrome, Partial Trisomy 21
Down Syndrome, Partial Trisomy 21 		19 0 19 1.00 0 0
CUI: C0432417
Disease: Trisomy 21, Meiotic Nondisjunction
Trisomy 21, Meiotic Nondisjunction 		19 0 19 1.00 0 0
CUI: C0751081
Disease: Trisomy 21, Mitotic Nondisjunction
Trisomy 21, Mitotic Nondisjunction 		19 0 19 1.00 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		4 0 2 9.5E-02 0 0
CUI: C0086664
Disease: Myelocele
Myelocele 		4 0 2 9.5E-02 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 2 9.5E-02 0 0
CUI: C0013604
Disease: Edema
Edema 		26 0 3 7.1E-02 0 0
CUI: C0151603
Disease: Anasarca
Anasarca 		26 0 3 7.1E-02 0 0
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity 		12 0 2 6.9E-02 0 0
CUI: C0344315
Disease: Depressed mood
Depressed mood 		13 0 2 6.7E-02 0 0
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		32 0 3 6.2E-02 0 0
CUI: C0920269
Disease: Microsatellite Instability
Microsatellite Instability 		15 0 2 6.2E-02 0 0
CUI: C1721098
Disease: Replication Error Phenotype
Replication Error Phenotype 		15 0 2 6.2E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 5.3E-02 0 0
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis 		1 0 1 5.3E-02 0 0
CUI: C0018944
Disease: Hematoma
Hematoma 		1 0 1 5.3E-02 0 0
CUI: C0027947
Disease: Neutropenia
Neutropenia 		21 0 2 5.3E-02 0 0
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		1 0 1 5.3E-02 0 0
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		1 0 1 5.3E-02 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		1 0 1 5.3E-02 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		1 0 1 5.3E-02 0 0
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden 		1 0 1 5.3E-02 0 0
CUI: C1834582
Disease: MYELOPROLIFERATIVE SYNDROME, TRANSIENT
MYELOPROLIFERATIVE SYNDROME, TRANSIENT 		1 0 1 5.3E-02 0 0
CUI: C1839161
Disease: Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis 		1 0 1 5.3E-02 0 0
CUI: C1845837
Disease: Dyserythropoietic Anemia with Thrombocytopenia
Dyserythropoietic Anemia with Thrombocytopenia 		1 0 1 5.3E-02 0 0