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Congenital high-molecular-weight kininogen deficiency
rareA rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis.
- Identifiers
- MONDO:0009234 OMIM:228960Orphanet:483
- Causal genes
- KNG1
- Also known as
- Fitzgerald trait · Fitzgerald trait kininogen deficiency, total, included · Flaujeac factor deficiency · Flaujeac trait, included · high molecular weight kininogen deficiency
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