Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.100 None 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		phenotype Finding 75 8 0.100 None 0
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 257 11 0.100 None 0
CUI: C4477095
Disease: Increased lactate dehydrogenase activity
Increased lactate dehydrogenase activity 		phenotype Finding 27 0.100 None 0
CUI: C4021818
Disease: Abnormality of the ovary
Abnormality of the ovary 		disease Anatomical Abnormality 8 1 0.100 None 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 122 24 0.100 None 0
CUI: C1853237
Disease: Isolated cases
Isolated cases 		phenotype Finding 111 0.100 None 0
CUI: C1839304
Disease: Decreased proportion of CD4-positive T cells
Decreased proportion of CD4-positive T cells 		phenotype Immune System Diseases; Hemic and Lymphatic Diseases Finding 19 0.100 None 0
CUI: C4025749
Disease: Abnormality of the spleen
Abnormality of the spleen 		disease Anatomical Abnormality 26 1 0.100 None 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas 		disease Anatomical Abnormality 13 1 0.100 None 0
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 196 76 0.100 None 0
CUI: C0021843
Disease: Intestinal Obstruction
Intestinal Obstruction 		disease Digestive System Diseases Disease or Syndrome 87 3 0.100 None 0
CUI: C4021634
Disease: Abnormality of bone marrow cell morphology
Abnormality of bone marrow cell morphology 		disease Anatomical Abnormality 15 0.100 None 0
CUI: C0149727
Disease: Abnormality of the lymph nodes
Abnormality of the lymph nodes 		phenotype Finding 3 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation 		phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C0281784
Disease: Benign Meningioma
Benign Meningioma 		disease Neoplasms; Nervous System Diseases Neoplastic Process 35 0.020 None < 0.001 2 2001 2008
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 130 71 0.010 None < 0.001 1 2003 2003
CUI: C4041089
Disease: Poorly differentiated sarcoma
Poorly differentiated sarcoma 		disease Neoplasms Neoplastic Process 11 0.010 None < 0.001 1 1988 1988
CUI: C4524190
Disease: High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements 		disease Neoplastic Process 3 0.010 None < 0.001 1 2018 2018
CUI: C2347753
Disease: Adult Pure Erythroid Leukemia
Adult Pure Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 5 0.010 None < 0.001 1 2017 2017
CUI: C0006160
Disease: Brenner Tumor
Brenner Tumor 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 14 1 0.010 None < 0.001 1 2016 2016
CUI: C4551593
Disease: Surface epithelial-stromal tumor
Surface epithelial-stromal tumor 		disease Neoplasms Neoplastic Process 6 1 0.010 None < 0.001 1 2016 2016
CUI: C4330531
Disease: Large Cell/Anaplastic Medulloblastoma
Large Cell/Anaplastic Medulloblastoma 		disease Neoplasms Neoplastic Process 1 0.010 None < 0.001 1 2006 2006
CUI: C4520841
Disease: Pure Erythroid Leukemia
Pure Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 13 0.010 None < 0.001 1 2017 2017
CUI: C0086692
Disease: Benign Neoplasm
Benign Neoplasm 		group Neoplasms Neoplastic Process 371 7 0.320 None 0.333 3 1993 2001