G6PD, glucose-6-phosphate dehydrogenase, 2539

N. diseases: 344; N. variants: 24
Source: BEFREE ×
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: C1387528
Disease: Acute haemolytic anaemia
Acute haemolytic anaemia 		disease Disease or Syndrome 3 0.100 None 1.000 13 1984 2019
CUI: C0472790
Disease: Chronic non-spherocytic hemolytic anemia
Chronic non-spherocytic hemolytic anemia 		disease Disease or Syndrome 2 4 0.080 None 0.875 8 2 1980 2011
CUI: C4727002
Disease: Chronic Hemolysis
Chronic Hemolysis 		disease Disease or Syndrome 6 1 0.060 None 1.000 6 1982 2008
CUI: C4732730
Disease: Blood spots
Blood spots 		disease Disease or Syndrome 117 0.050 None 1.000 5 2010 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.040 None 1.000 4 1989 2019
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		disease Disease or Syndrome 6 1 0.030 None 1.000 3 1984 1994
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		disease Neoplastic Process 860 154 0.020 None 1.000 2 1985 1985
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.020 None 1.000 2 2012 2019
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.020 None 1.000 2 2017 2019
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		disease Disease or Syndrome 6 0.010 None < 0.001 1 2009 2009
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		disease Congenital Abnormality 135 3 0.010 None 1.000 1 2009 2009
CUI: C0085662
Disease: Macrocytosis
Macrocytosis 		disease Disease or Syndrome 13 0.010 None 1.000 1 1993 1993
CUI: C0302847
Disease: major affective disorder
major affective disorder 		disease Mental or Behavioral Dysfunction 4 2 0.010 None 1.000 1 1999 1999
CUI: C0426359
Disease: Urinary symptoms
Urinary symptoms 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2010 2010
CUI: C0543968
Disease: Cone dysfunction syndrome
Cone dysfunction syndrome 		disease Disease or Syndrome 25 2 0.010 None 1.000 1 1981 1981
CUI: C0746365
Disease: malaria relapse
malaria relapse 		disease Disease or Syndrome 1 0.010 None < 0.001 1 2016 2016
CUI: C0747820
Disease: Malaria, antepartum
Malaria, antepartum 		disease Disease or Syndrome 15 0.010 None 1.000 1 2003 2003
CUI: C0850672
Disease: hereditary anemia
hereditary anemia 		disease Disease or Syndrome 4 0.010 None 1.000 1 1993 1993
CUI: C0948201
Disease: Alloimmunisation
Alloimmunisation 		disease Disease or Syndrome 63 1 0.010 None 1.000 1 2018 2018
CUI: C0948379
Disease: Impaired insulin secretion
Impaired insulin secretion 		disease Disease or Syndrome 88 14 0.010 None 1.000 1 2010 2010
CUI: C1283397
Disease: Deficiency of acetylcholinesterase
Deficiency of acetylcholinesterase 		disease Disease or Syndrome 5 0.010 None 1.000 1 1977 1977
CUI: C1291611
Disease: Deficiency of glucose-6-phosphate isomerase
Deficiency of glucose-6-phosphate isomerase 		disease Disease or Syndrome 1 0.010 None 1.000 1 2004 2004
CUI: C1827377
Disease: Slow acetylator due to N-acetyltransferase enzyme variant
Slow acetylator due to N-acetyltransferase enzyme variant 		disease Disease or Syndrome 20 8 0.010 None 1.000 1 1982 1982
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia 		disease Neoplastic Process 236 4 0.010 None 1.000 1 1983 1983
CUI: C3841459
Disease: Hb H disease
Hb H disease 		disease Disease or Syndrome 10 2 0.010 None 1.000 1 1980 1980