class V glucose-6-phosphate dehydrogenase deficiency

disease
On this page

Also known as G6PD class V variant anaemiaG6PD class V variant anemiaG6PD deficiencyglucose-6-phosphate dehydrogenase deficiency class V variant anaemiaglucose-6-phosphate dehydrogenase deficiency class V variant anemia

Summary

class V glucose-6-phosphate dehydrogenase deficiency (MONDO:0040671) is a disease and 21 clinical trials. Top therapeutic interventions include primaquine, chloroquine, and tafenoquine. A subtype of G6PD deficiency — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 21

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameclass V glucose-6-phosphate dehydrogenase deficiency
Mondo IDMONDO:0040671
Orphanet362
SNOMED CT80963002
UMLSC0272060
MedGen543772
GARD0027958
Is cancer (heuristic)no

Also known as: G6PD class V variant anaemia · G6PD class V variant anemia · G6PD deficiency · glucose-6-phosphate dehydrogenase deficiency class V variant anaemia · glucose-6-phosphate dehydrogenase deficiency class V variant anemia

Disease family

This is a subtype of G6PD deficiency. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › disease of genetic or genomic mechanism › hereditary diseaseinborn errors of metabolisminborn carbohydrate metabolic disorderG6PD deficiencyclass V glucose-6-phosphate dehydrogenase deficiency

Related subtypes (2): favism, anemia, nonspherocytic hemolytic, due to G6PD deficiency

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 21.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified14
PHASE44
PHASE21
EARLY_PHASE11
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07468513PHASE4RECRUITINGPrimaquine for Vivax Malaria in G6PD Intermediate and Deficient Cases.
NCT02434952PHASE4COMPLETEDSafety and Tolerability of Low Dose Primaquine
NCT03337152PHASE4TERMINATEDAssessing a Risk Model for G6PD Deficiency
NCT04088513PHASE4UNKNOWNSafety and Efficacy of Aspirin in Stroke Patients With Glucose-6-phosphate Dehydrogenase Deficiency (SAST)
NCT03529396PHASE2COMPLETEDSafety and Efficacy of Different Regimens of Primaquine on Vivax Malaria Treatment in G6PD Deficient Patients
NCT04073953PHASE1COMPLETEDPrimaquine Enantiomers in G6PD Deficient Human Volunteers
NCT02937376EARLY_PHASE1UNKNOWNEffects of N-acetyl Cystein (NAC) Supplementation in G6PD Deficient Individuals After Acute Exercise
NCT03655223Not specifiedENROLLING_BY_INVITATIONEarly Check: Expanded Screening in Newborns
NCT01931644Not specifiedCOMPLETEDAt-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions
NCT02937363Not specifiedCOMPLETEDEffects of Alpha Lipoic Acid Supplementation in G6PD Deficient Individuals After Acute Exercise
NCT04010695Not specifiedCOMPLETEDValidation of Diagnostics to Identify Glucose-6-phosphate Dehydrogenase Activity in the US
NCT04033640Not specifiedCOMPLETEDEvaluation of a Diagnostic to Identify Glucose-6-phosphate Dehydrogenase (G6PD) Deficiency in Brazil
NCT04054661Not specifiedCOMPLETEDValidation of a Diagnostic Test for Glucose-6-phosphate Dehydrogenase (G6PD) Deficiency in Anti-coagulated Blood
NCT04081272Not specifiedCOMPLETEDEffect of G6PD Deficiency on Red Blood Cell Storage
NCT04146246Not specifiedCOMPLETEDComparative Evaluation of the FINDER Instrument and FINDER G6PD Cartridge in Adults and Neonates
NCT05026489Not specifiedUNKNOWNG6PD Deficiency in Infarction Patients in Shaanxi Province
NCT05096702Not specifiedUNKNOWNOperational Feasibility of Appropriate Radical Cure of Plasmodium Vivax With Tafenoquine or Primaquine After Quantitative G6PD Testing in Brazil
NCT05571748Not specifiedUNKNOWNOxidative Stress, Carbohydrate Metabolism Disorders and G6PD Deficiency
NCT05753150Not specifiedCOMPLETEDOperational Feasibility of Appropriate Plasmodium Vivax Radical Cure After G6PD Testing in Thailand
NCT05874271Not specifiedCOMPLETEDShort Course Primaquine for the Radical Cure of P. Vivax - Papua New Guinea
NCT05879224Not specifiedCOMPLETEDShort Course Primaquine for the Radical Cure of P. Vivax Malaria - Indonesia

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
PRIMAQUINE415
CHLOROQUINE42
TAFENOQUINE42
CYSTEINE41
SODIUM CHROMATE CR 5141
LIPOIC ACID, ALPHA32