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Factor X Deficiency MeSH Descriptor Data 2022


MeSH Heading
Factor X Deficiency
Tree Number(s)
C15.378.100.100.320
C15.378.100.141.320
C15.378.463.320
C16.320.099.320
Unique ID
D005171
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005171
Annotation
a blood coag disord
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.
Entry Version
FACTOR X DEFIC
Entry Term(s)
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
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
Date Established
1991/01/01
Date of Entry
1999/01/01
Revision Date
2017/05/02
Factor X Deficiency Preferred
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