| Descriptor English: | Factor X Deficiency | ||||||
| Descriptor Spanish: |
Deficiencia del Factor X
| ||||||
| Descriptor Portuguese: | Deficiência do Fator X | ||||||
| Descriptor French: | Déficit en facteur X | ||||||
| Entry term(s): |
Deficiencies, Factor 10 Deficiencies, Factor Ten Deficiencies, Factor X Deficiency, Factor 10 Deficiency, Factor Ten Deficiency, Factor X Deficiency, Stuart Prower Deficiency, Stuart Prower Factor Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Factor 10 Deficiencies Factor 10 Deficiency Factor Ten Deficiencies Factor Ten Deficiency Factor X Deficiencies Stuart Prower Deficiency Stuart Prower Factor Deficiency Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Ten Deficiencies, Factor |
||||||
| Tree number(s): |
C15.378.100.100.320 C15.378.100.141.320 C15.378.463.320 C16.320.099.320 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005171 | ||||||
| Scope note: | 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. |
||||||
| Annotation: | a blood coag disord |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Public MeSH Note: | 91; was see under HYPOPROTHROMBINEMIAS 1975-90 |
||||||
| Online Note: | search HYPOPROTHROMBINEMIAS 1966-74 |
||||||
| History Note: | 91(75); was see under HYPOPROTHROMBINEMIAS 1975-90 |
||||||
| Entry Version: | FACTOR X DEFIC |
||||||
| DeCS ID: | 5271 | ||||||
| Unique ID: | D005171 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2017/05/02 |
|
|
Factor X Deficiency
- Preferred
| Concept UI |
M0008155 |
| Scope note | 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. |
| Preferred term | Factor X Deficiency |
| Entry term(s) |
Deficiencies, Factor 10 Deficiencies, Factor Ten Deficiencies, Factor X Deficiency, Factor 10 Deficiency, Factor Ten Deficiency, Factor X Deficiency, Stuart Prower Deficiency, Stuart Prower Factor Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Factor 10 Deficiencies Factor 10 Deficiency Factor Ten Deficiencies Factor Ten Deficiency Factor X Deficiencies Stuart Prower Deficiency Stuart Prower Factor Deficiency Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Ten Deficiencies, Factor |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
