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: C0269972
Disease: Postpartum cardiomyopathy
Postpartum cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2007 2007
CUI: C0276089
Disease: Pneumonia due to Escherichia coli
Pneumonia due to Escherichia coli 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2008 2008
CUI: C0858213
Disease: vascular aneurysm
vascular aneurysm 		disease Anatomical Abnormality 5 0.010 None 1.000 1 2012 2012
CUI: C1304193
Disease: Chronic autoimmune urticaria
Chronic autoimmune urticaria 		disease Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C1333294
Disease: ALK positive large B-cell lymphoma
ALK positive large B-cell lymphoma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 5 0.010 None 1.000 1 2013 2013
CUI: C1963788
Disease: Peripheral nerve lesion
Peripheral nerve lesion 		disease Nervous System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0011630
Disease: Dermatomycoses
Dermatomycoses 		group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0018852
Disease: Heavy Chain Disease
Heavy Chain Disease 		group Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 6 0.010 None 1.000 1 2010 2010
CUI: C1697846
Disease: Psoriatic conditions
Psoriatic conditions 		disease Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C2931027
Disease: Neutropenia, severe chronic
Neutropenia, severe chronic 		disease Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None 1.000 1 1999 1999
CUI: C0349571
Disease: Pleomorphic adenoma of parotid gland
Pleomorphic adenoma of parotid gland 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 7 0.010 None 1.000 1 2015 2015
CUI: C2677362
Disease: Alveolar capillary dysplasia
Alveolar capillary dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 7 0.010 None 1.000 1 2019 2019
CUI: C2861580
Disease: Chronic myeloid leukemia, BCR/ABL-positive
Chronic myeloid leukemia, BCR/ABL-positive 		disease Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2014 2014
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells 		phenotype Finding 7 0.100 None 0
CUI: C0032109
Disease: Plasma cell mastitis
Plasma cell mastitis 		disease Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 8 0.020 None 1.000 2 2018 2020
CUI: C4518436
Disease: Anaplastic lymphoma kinase positive anaplastic large cell lymphoma
Anaplastic lymphoma kinase positive anaplastic large cell lymphoma 		disease Neoplastic Process 8 0.020 None 1.000 2 2004 2011
CUI: C0279619
Disease: Adult Acute Erythroid Leukemia
Adult Acute Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2016 2016
CUI: C1260326
Disease: Dendritic Cell Sarcoma, Interdigitating
Dendritic Cell Sarcoma, Interdigitating 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 2 0.010 None 1.000 1 2018 2018
CUI: C1332937
Disease: Childhood Acute Erythroid Leukemia
Childhood Acute Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2016 2016
CUI: C1955634
Disease: Kaposi's sarcoma-associated herpesvirus infection
Kaposi's sarcoma-associated herpesvirus infection 		disease Disease or Syndrome 8 0.010 None 1.000 1 2007 2007
CUI: C4330043
Disease: Gingival Squamous Cell Carcinoma
Gingival Squamous Cell Carcinoma 		disease Neoplastic Process 8 0.010 None 1.000 1 2017 2017
CUI: C0024054
Disease: Lown-Ganong-Levine Syndrome
Lown-Ganong-Levine Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2013 2013
CUI: C0268547
Disease: Argininosuccinic Aciduria
Argininosuccinic Aciduria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 9 84 0.010 None 1.000 1 2019 2019
CUI: C0003969
Disease: Ascorbic Acid Deficiency
Ascorbic Acid Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 10 0.010 None 1.000 1 2019 2019
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		disease Cardiovascular Diseases Anatomical Abnormality 10 2 0.010 None 1.000 1 2010 2010