Pyridoxine deficiency anemia
disease diseaseOn this page
Also known as B6 deficiencies, vitaminB6 deficiency, vitaminB6 vitamin deficienciesB6 vitamin deficiencydeficiencies, B6 vitamindeficiencies, vitamin B6deficiency, B6 vitamindeficiency, pyridoxinedeficiency, vitamin B 6deficiency, vitamin B6pyridoxine deficiencypyridoxine Deficincyvitamin B6 deficienciesvitamin B6 deficiencyvitamin deficiencies, B6vitamin deficiency, B6
Summary
Pyridoxine deficiency anemia (MONDO:0004574) is a disease and 3 clinical trials. Top therapeutic interventions include pyridoxine and leucine. A subtype of vitamin B deficiency — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 3
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | pyridoxine deficiency anemia |
| Mondo ID | MONDO:0004574 |
| MeSH | D026681 |
| DOID | DOID:8455 |
| NCIT | C85221 |
| SNOMED CT | 86448001 |
| UMLS | C0272013 |
| MedGen | 543733 |
| GARD | 0004616 |
| Is cancer (heuristic) | no |
Also known as: B6 deficiencies, vitamin · B6 deficiency, vitamin · B6 vitamin deficiencies · B6 vitamin deficiency · deficiencies, B6 vitamin · deficiencies, vitamin B6 · deficiency, B6 vitamin · deficiency, pyridoxine · deficiency, vitamin B 6 · deficiency, vitamin B6 · pyridoxine deficiency · pyridoxine Deficincy · vitamin B6 deficiencies · vitamin B6 deficiency · vitamin deficiencies, B6 · vitamin deficiency, B6
Disease family
This is a subtype of vitamin B 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 › nutritional disorder › nutritional deficiency disease › vitamin deficiency disorder › vitamin B deficiency › pyridoxine deficiency anemia
Related subtypes (2): beriberi, vitamin B12 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: 3.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01128244 | PHASE2/PHASE3 | COMPLETED | Vitamin B6 Effects for Women Taking Birth Control Pills |
| NCT00877812 | Not specified | COMPLETED | Vitamin B6 Dependence of One-Carbon Metabolism |
| NCT03444155 | Not specified | COMPLETED | Natural Versus Synthetic Vitamin B Complexes in Human |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| PYRIDOXINE | 4 | 1 |
| LEUCINE | 3 | 2 |
Related Atlas pages
- Drugs: Pyridoxine