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: C0276721
Disease: Phaeohyphomycosis
Phaeohyphomycosis 		disease Infections Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C0276279
Disease: Mink parvovirus infection
Mink parvovirus infection 		disease Infections Disease or Syndrome 10 0.010 None 1.000 1 2019 2019
CUI: C0017672
Disease: Glossalgia
Glossalgia 		phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Sign or Symptom 11 0.010 None 1.000 1 2017 2017
CUI: C2242704
Disease: Chronic myeloid leukaemia transformation
Chronic myeloid leukaemia transformation 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 11 0.010 None < 0.001 1 2007 2007
CUI: C4546431
Disease: Exacerbation of allergic asthma
Exacerbation of allergic asthma 		disease Disease or Syndrome 11 0.010 None 1.000 1 2020 2020
CUI: C0406486
Disease: Ocular Rosacea
Ocular Rosacea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C0474368
Disease: Labor Pain
Labor Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 12 1 0.010 None 1.000 1 2019 2019
CUI: C2721566
Disease: Meniscal degeneration
Meniscal degeneration 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 13 0.010 None 1.000 1 2008 2008
CUI: C3469526
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP F
FANCONI ANEMIA, COMPLEMENTATION GROUP F 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 13 6 0.010 None 1.000 1 2012 2012
CUI: C0400807
Disease: Stress ulcer of stomach
Stress ulcer of stomach 		disease Digestive System Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2019 2019
CUI: C2741638
Disease: Stress ulcer
Stress ulcer 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2019 2019
CUI: C1864040
Disease: Cerebral Cavernous Malformations 3
Cerebral Cavernous Malformations 3 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 15 9 0.010 None 1.000 1 2009 2009
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion 		disease Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C3873363
Disease: Acute pulmonary thromboembolism
Acute pulmonary thromboembolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 15 0.010 None 1.000 1 2019 2019
CUI: C2242710
Disease: Intra-Abdominal Hypertension
Intra-Abdominal Hypertension 		disease Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 17 0.010 None 1.000 1 2016 2016
CUI: C0151565
Disease: Hemorrhagic colitis
Hemorrhagic colitis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C0268251
Disease: Gaucher Disease, Type 3 (disorder)
Gaucher Disease, Type 3 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 26 0.010 None 1.000 1 2015 2015
CUI: C1455780
Disease: Aortic valve sclerosis
Aortic valve sclerosis 		disease Nutritional and Metabolic Diseases; Cardiovascular Diseases Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0015974
Disease: Periodic fever
Periodic fever 		disease Disease or Syndrome 19 5 0.010 None 1.000 1 2011 2011
CUI: C0428796
Disease: Senile sclerosis of aortic cusp
Senile sclerosis of aortic cusp 		disease Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19 5 0.010 None 1.000 1 2017 2017
CUI: C1262117
Disease: Fungal keratitis
Fungal keratitis 		disease Pathological Conditions, Signs and Symptoms; Infections; Eye Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2017 2017
CUI: C1319466
Disease: Barber Say syndrome
Barber Say syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 21 4 0.010 None 1.000 1 2012 2012
CUI: C3468041
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP C
FANCONI ANEMIA, COMPLEMENTATION GROUP C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 22 73 0.010 None 1.000 1 2017 2017
CUI: C0278147
Disease: Radicular pain
Radicular pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 23 5 0.010 None 1.000 1 2019 2019