Structured Summary
Abstract
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
MeSH Record
Classification
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MeSH Record
Synonyms
20 entry terms
- Deficiency, Factor 10
- Deficiency, Factor Ten
- Deficiency, Factor X
- Deficiency, Stuart-Prower
- Deficiency, Stuart-Prower Factor
- Factor 10 Deficiency
- Factor Ten Deficiency
- Stuart-Prower Deficiency
- Stuart-Prower Factor Deficiency
- Deficiencies, Factor 10
- Deficiencies, Factor Ten
- Deficiencies, Factor X
- Deficiency, Stuart Prower
- Deficiency, Stuart Prower Factor
- Factor 10 Deficiencies
- Factor Ten Deficiencies
- Factor X Deficiencies
- Stuart Prower Deficiency
- Stuart Prower Factor Deficiency
- Ten Deficiencies, Factor
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
a blood coag disord
MeSH Record
History Note
91(75); was see under HYPOPROTHROMBINEMIAS 1975-90
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Factor X Deficiency. Medical Subject Headings (MeSH). 2026. Unique ID D005171. http://id.nlm.nih.gov/mesh/2026/D005171
- Factor X Deficiency. In: Wikipedia. https://en.wikipedia.org/wiki/Factor_X_deficiency
- Factor X Deficiency. In: Wikidata. https://www.wikidata.org/wiki/Q18555036