factor X deficiency
Information
- Disease name
- factor X deficiency
- Disease ID
- DOID:2222
- Description
- "A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood." [url:https\://rarediseases.org/rare-diseases/factor-x-deficiency/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00930176 | Completed | Phase 3 | A Study Investigating Treatment Factor X in People With Factor X Deficiency | January 2010 | November 2013 |
| NCT01721681 | Completed | Phase 3 | A Study to Investigate Bio Product Laboratory Ltd (BPL's) Factor X in the Prophylaxis of Bleeding in Children <12 Years | April 2015 | October 2016 |
| NCT03655223 | Enrolling by invitation | Early Check: Expanded Screening in Newborns | October 15, 2018 | December 31, 2025 | |
| NCT01086852 | Terminated | Phase 3 | Safety & Efficacy of BPL's High Purity FACTOR X in Treatment of Factor X Deficient Subjects Undergoing Surgery | March 2011 | January 2014 |
- Disase is a (Disease Ontology)
- DOID:1247
- Cross Reference ID (Disease Ontology)
- GARD:6404
- Cross Reference ID (Disease Ontology)
- MESH:D005171
- Cross Reference ID (Disease Ontology)
- MIM:227600
- Cross Reference ID (Disease Ontology)
- NCI:C131632
- Cross Reference ID (Disease Ontology)
- ORDO:328
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:76642003
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0015519
- Exact Synonym (Disease Ontology)
- disease, Stuart-Prower
- MeSH unique ID (MeSH (Medical Subject Headings))
- D005171