pancytopenia
Information
- Disease name
- pancytopenia
- Disease ID
- DOID:12450
- Description
- "An anemia that is characterized by a reduction in the number of red blood cells, white blood cells, and platelets." [url:https\://en.wikipedia.org/wiki/Pancytopenia]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00000597 | Completed | Phase 3 | Multi-Center Trial of Anti-Thymocyte Globulin in Treatment of Aplastic Anemia and Other Hematologic Disorders | March 1982 | December 1988 |
| NCT00001214 | Completed | Collection of Blood From Patients With Pancytopenia | April 30, 1986 | August 17, 2020 | |
| NCT00001398 | Completed | Phase 1 | Stem Cell Factor Medication for Aplastic Anemia | October 1993 | June 2002 |
| NCT00001399 | Completed | Phase 1 | Gene Therapy for the Treatment of Fanconi's Anemia Type C | December 3, 1993 | February 11, 2009 |
| NCT00260689 | Completed | Phase 2 | Three Immunosuppressive Treatment Regimens for Severe Aplastic Anemia | November 28, 2005 | May 4, 2016 |
| NCT01187017 | Completed | Phase 1/Phase 2 | A Pilot Study of Fludarabine Plus Cyclophosphamide in Refractory Severe Aplastic Anemia | August 2010 | July 2012 |
| NCT01193283 | Completed | Phase 1/Phase 2 | Cyclophosphamide Plus Cyclosporine in Treatment-Naive Severe Aplastic Anemia | August 2010 | September 2014 |
| NCT05473650 | Not yet recruiting | Spectrum of Hematological Disorders in Pediatrics | September 1, 2022 | November 1, 2023 | |
| NCT03521947 | Unknown status | Management of Childhood Pancytopenia | June 1, 2018 | December 1, 2019 |
- Disase is a (Disease Ontology)
- DOID:2355
- Cross Reference ID (Disease Ontology)
- ICD10CM:D61.81
- Cross Reference ID (Disease Ontology)
- ICD9CM:284.1
- Cross Reference ID (Disease Ontology)
- MESH:D010198
- Cross Reference ID (Disease Ontology)
- NCI:C34889
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:127034005
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0030312
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0001876
- MeSH unique ID (MeSH (Medical Subject Headings))
- D010198