pure red-cell aplasia
Information
- Disease name
- pure red-cell aplasia
- Disease ID
- DOID:1340
- Description
- "A congenital hypoplastic anemia that is characterized by a normocytic normochromic anemia with severe reticulocytopenia and marked reduction or absence of erythroid precursors from the bone marrow." [url:https\://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142432/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00004378 | Completed | N/A | Stem Cell Transplantation (SCT) for Genetic Diseases | January 1995 | |
| NCT00211042 | Completed | A Study of Patients With Pure Red Cell Aplasia Associated With Recombinant Human Erythropoietin Treatment | February 2004 | December 2006 | |
| NCT00211068 | Completed | A Study of Risk Factors for Anti-erythropoietin Antibody Positive Pure Red Cell Aplasia Among Patients With Chronic Kidney Disease Receiving Epoetin Alfa | March 2004 | March 2006 | |
| NCT00391287 | Completed | Surveillance Study to Estimate the Incidence of Pure Red Blood Cell Aplasia Among Patients With Chronic Kidney Failure | June 2006 | December 2010 |
- Disase is a (Disease Ontology)
- DOID:1342
- Cross Reference ID (Disease Ontology)
- GARD:7504
- Cross Reference ID (Disease Ontology)
- MESH:D012010
- Cross Reference ID (Disease Ontology)
- NCI:C34974
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:191252000
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0034902
- Exact Synonym (Disease Ontology)
- primary red cell aplasia
- Exact Synonym (Disease Ontology)
- pure red cell aplasia
- Exact Synonym (Disease Ontology)
- Red cell hypoplasia