(Q55781893)
English
congenital high-molecular-weight kininogen deficiency
rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis
- Fitzgerald Trait
- HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY
- HMWK
- FITZGERALD TRAIT KININOGEN DEFICIENCY, TOTAL, INCLUDED
- Flaujeac factor deficiency
- Kininogen Deficiency, High Molecular Weight and Low Molecular Weight
- Flaujeac Trait
- KININOGEN DEFICIENCY, HIGH MOLECULAR WEIGHT AND LOW MOLECULAR WEIGHT, INCLUDED
- High-molecular-weight kininogen deficiency, congenital
- Kininogen Deficiency, Total
- Williams Trait
- WILLIAMS TRAIT, INCLUDED
- HMWK Deficiency
- Kininogen Deficiency, High Molecular Weight
- FLAUJEAC TRAIT, INCLUDED
- high molecular weight kininogen deficiency
Statements
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286.9
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C98946
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Identifiers
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