Hereditary factor XI deficiency disease
- Synonyms
- Congenital factor XI deficiency; PTA deficiency; Plasma thromboplastin antecedent deficiency; Rosenthal syndrome
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Autosomal dominant inheritance (Orphanet)
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Abnormal bleeding
Abnormal bleeding
- MedGen UID: 264316
- Concept ID: C1458140
- Finding: Pathologic Function
Abnormality of blood and blood-forming tissues
- Prolonged partial thromboplastin time
Prolonged partial thromboplastin time
- MedGen UID: 66815
- Concept ID: C0240671
- Finding: Finding
Abnormality of blood and blood-forming tissues
- Reduced factor XI activity
Reduced factor XI activity
- MedGen UID: 1368629
- Concept ID: C4317093
- Finding: Finding
Abnormality of blood and blood-forming tissues
- Abnormal bleeding
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