Factor X Deficiency, Congenital
Common Name(s)
Factor X Deficiency, Congenital
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Factor X Deficiency, Congenital" for support, advocacy or research.
How do you compare to others with this condition?
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Factor X Deficiency, Congenital" for support, advocacy or research.
Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Factor X Deficiency, Congenital can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Scientific Literature
Articles from the PubMed Database
Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Factor X Deficiency, Congenital" returned 0 free, full-text research articles on human participants.
No free, full-text research articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Factor X Deficiency, Congenital".
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Factor X Deficiency, Congenital" returned 0 free, full-text review articles on human participants.
No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Factor X Deficiency, Congenital".
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/condition/factor-vii-deficiency
https://ghr.nlm.nih.gov/condition/congenital-afibrinogenemia
https://ghr.nlm.nih.gov/condition/factor-v-deficiency
https://ghr.nlm.nih.gov/gene/F10
https://ghr.nlm.nih.gov/condition/complement-factor-i-deficiency
https://ghr.nlm.nih.gov/condition/factor-xi-deficiency
https://ghr.nlm.nih.gov/condition/factor-xiii-deficiency
https://ghr.nlm.nih.gov/condition/prekallikrein-deficiency
https://ghr.nlm.nih.gov/condition/porphyria
https://ghr.nlm.nih.gov/gene/HAX1
https://ghr.nlm.nih.gov/condition/severe-congenital-neutropenia
https://ghr.nlm.nih.gov/condition/congenital-leptin-deficiency
https://ghr.nlm.nih.gov/condition/hereditary-antithrombin-deficiency
https://ghr.nlm.nih.gov/condition/x-linked-creatine-deficiency
https://ghr.nlm.nih.gov/condition/x-linked-agammaglobulinemia
https://ghr.nlm.nih.gov/gene/LEP
https://ghr.nlm.nih.gov/condition/x-linked-infantile-nystagmus
https://ghr.nlm.nih.gov/condition/autosomal-recessive-congenital-methemoglobinemia
https://ghr.nlm.nih.gov/gene/ZIC3
There are currently no related results available in GeneReviews.
There are currently no related results available in Genetic Testing Registry.
Clinical Trial Information This information is provided by ClinicalTrials.gov
Condition Summary: Factor 10 Deficiency

Finding the right clinical trial for Factor X Deficiency, Congenital can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.