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Factor XI Deficiency MeSH Descriptor Data 2021


MeSH Heading
Factor XI Deficiency
Tree Number(s)
C15.378.100.100.325
C15.378.100.141.325
C15.378.463.325
C16.320.099.325
Unique ID
D005173
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D005173
Annotation
a blood coag disord
Scope Note
A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.
Entry Version
FACTOR XI DEFIC
Entry Term(s)
Deficiency, Factor 11
Deficiency, Factor Eleven
Deficiency, Factor XI
Factor 11 Deficiency
Factor Eleven Deficiency
Hemophilia C
Plasma Thromboplastin Antecedent Deficiency
Rosenthal Syndrome
Rosenthal's Syndrome
See Also
Factor XI
Public MeSH Note
1973
History Note
1973(1966)
Date Established
1973/01/01
Date of Entry
1999/01/01
Revision Date
2017/05/02
Factor XI Deficiency Preferred
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