Disease_Mapped_To_Gene CTRP Terminology Pediatric Hematology-Oncology Terminology CTRP Biomarker Terminology CTRP Molecular Genetic Biomarker Terminology CPTAC Terminology CPTAC Medical Conditions Codelist CPTAC Codelists Terminology Cellosaurus Disease Terminology G6PD Gene Congenital Metabolic Disorder Rare Non-Neoplastic Disorder NICHD Terminology Glucose-6-Phosphate Dehydrogenase Deficiency G-6-PD Variant Enzyme Deficiency Anemia NICHD An X-linked recessive disorder caused by mutations in the G6PD gene. It is characterized by subnormal activity of glucose-6-phosphate dehydrogenase. Patients develop hemolytic anemia, usually in response to infection or exposure to food, drugs, or other substances. An X-linked recessive inherited disorder caused by mutations in the G6PD gene. It is characterized by the absence or presence of very low levels of glucose-6-phosphate dehydrogenase. Patients develop hemolytic anemia usually in response to infection or exposure to drugs. C98933 Cellosaurus Disease or Syndrome Glucose-6-Phosphate Dehydrogenase Deficiency G6PD G6PD Deficiency Glucose-6-Phosphate Dehydrogenase Deficiency Glucose-6-Phosphate Dehydrogenase Deficiency CPTAC C2939465 CTRP Neonatal Research Network Terminology