COX8A, cytochrome c oxidase subunit 8A, 1351

N. diseases: 526; N. variants: 2
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.090 None 1.000 9 2001 2019
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia 		disease Disease or Syndrome 7 2 0.080 None 1.000 8 2001 2019
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.050 None 1.000 5 2003 2019
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		disease Disease or Syndrome 985 56 0.040 None 1.000 4 1988 1991
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site 		disease Disease or Syndrome 467 14 0.030 None 1.000 3 2017 2019
CUI: C2873785
Disease: Deficiency of factor V [labile]
Deficiency of factor V [labile] 		disease Disease or Syndrome 3 0.030 None 1.000 3 1976 2013
CUI: C0272342
Disease: Familial multiple factor deficiency syndrome, type I
Familial multiple factor deficiency syndrome, type I 		disease Disease or Syndrome 4 0.020 None 1.000 2 2011 2017
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		disease Neoplastic Process 860 154 0.020 None 1.000 2 2007 2018
CUI: C1854510
Disease: Abnormality of the cranial nerves
Abnormality of the cranial nerves 		disease Anatomical Abnormality 17 2 0.020 None 1.000 2 2010 2017
CUI: C1959635
Disease: Parvovirus B19 (disease)
Parvovirus B19 (disease) 		disease Disease or Syndrome 59 0.020 None 1.000 2 1997 2005
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		disease Disease or Syndrome 695 94 0.020 None 1.000 2 1990 1991
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency 		disease Disease or Syndrome 6 9 0.020 None 1.000 2 1979 2017
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		disease Congenital Abnormality 181 4 0.010 None 1.000 1 1991 1991
CUI: C0028259
Disease: Nodule
Nodule 		phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2018 2018
CUI: C0040253
Disease: Tinea of perianal region
Tinea of perianal region 		disease Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders 		group Mental or Behavioral Dysfunction 360 56 0.010 None 1.000 1 2019 2019
CUI: C0240225
Disease: Liver mass
Liver mass 		phenotype Disease or Syndrome 36 0.010 None 1.000 1 2018 2018
CUI: C0243066
Disease: Atresia
Atresia 		disease Congenital Abnormality 44 1 0.010 None 1.000 1 2017 2017
CUI: C0346989
Disease: Secondary malignant neoplasm of peritoneum
Secondary malignant neoplasm of peritoneum 		disease Neoplastic Process 58 2 0.010 None 1.000 1 2019 2019
CUI: C0542259
Disease: Morphological abnormality of the vestibule of the inner ear
Morphological abnormality of the vestibule of the inner ear 		group Anatomical Abnormality 2 0.010 None 1.000 1 2017 2017
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		disease Disease or Syndrome 60 14 0.010 None 1.000 1 1998 1998
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		phenotype Neoplastic Process 384 40 0.010 None 1.000 1 2017 2017
CUI: C0678329
Disease: drug substitution (abuse)
drug substitution (abuse) 		disease Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2012 2012
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease Disease or Syndrome 321 67 0.010 None 1.000 1 2017 2017
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder 		phenotype Disease or Syndrome 171 1 0.010 None 1.000 1 2019 2019