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: C1532710
Disease: Isoniazid resistant tuberculosis
Isoniazid resistant tuberculosis 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0344503
Disease: Congenital epiblepharon
Congenital epiblepharon 		disease Congenital Abnormality 2 0.100 None 0
CUI: C0041332
Disease: Tuberculosis of other urinary organs
Tuberculosis of other urinary organs 		group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C1532782
Disease: Rifampicin resistant tuberculosis
Rifampicin resistant tuberculosis 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0022415
Disease: Joint Tuberculosis
Joint Tuberculosis 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 6 0.020 None 1.000 2 2015 2018
CUI: C0026919
Disease: Mycobacterium Infections, Nontuberculous
Mycobacterium Infections, Nontuberculous 		group Infections Disease or Syndrome 7 0.010 None 1.000 1 2020 2020
CUI: C0235592
Disease: Cervical lymphadenopathy
Cervical lymphadenopathy 		disease Hemic and Lymphatic Diseases Disease or Syndrome 11 1 0.010 None 1.000 1 2004 2004
CUI: C0349702
Disease: Corneal Scar
Corneal Scar 		phenotype Eye Diseases; Nervous System Diseases; Wounds and Injuries Finding 14 0.100 None 0
CUI: C1849341
Disease: Triangular mouth
Triangular mouth 		phenotype Finding 14 0.100 None 0
CUI: C0431384
Disease: Colpocephaly
Colpocephaly 		disease Nervous System Diseases Congenital Abnormality 17 2 0.100 None 0
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 29 8 0.010 None 1.000 1 2004 2004
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 35 12 0.100 None 0
CUI: C2959467
Disease: Tuberculous pleural effusion
Tuberculous pleural effusion 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 36 0.010 None 1.000 1 2016 2016
CUI: C0206525
Disease: Tuberculosis, Drug-Resistant
Tuberculosis, Drug-Resistant 		disease Infections Disease or Syndrome 37 0.040 None 1.000 4 2015 2019
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 47 3 0.010 None 1.000 1 2020 2020
CUI: C0024205
Disease: Lymphadenitis
Lymphadenitis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 55 2 0.010 None 1.000 1 2015 2015
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary 		disease Infections Disease or Syndrome 58 21 0.070 None 0.857 7 2016 2019
CUI: C0026916
Disease: Mycobacterium avium-intracellulare Infection
Mycobacterium avium-intracellulare Infection 		disease Infections Disease or Syndrome 58 5 0.010 None < 0.001 1 1996 1996
CUI: C0041326
Disease: Pleural Tuberculosis
Pleural Tuberculosis 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 59 0.020 None 1.000 2 2006 2014
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 60 11 0.100 None 0
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		disease Cardiovascular Diseases Disease or Syndrome 60 5 0.100 None 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 61 7 0.100 None 0
CUI: C0206526
Disease: Tuberculosis, Multidrug-Resistant
Tuberculosis, Multidrug-Resistant 		disease Infections Disease or Syndrome 67 8 0.100 None 1.000 11 1999 2018
CUI: C0041318
Disease: Tuberculosis, Meningeal
Tuberculosis, Meningeal 		disease Infections; Nervous System Diseases Disease or Syndrome 68 10 0.030 None 1.000 3 2014 2017
CUI: C0426848
Disease: Sacral dimple
Sacral dimple 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities Finding 69 11 0.100 None 0