congenital high-molecular-weight kininogen deficiency ^{الإنجليزية} (Q5440596)

rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis ^{الإنجليزية}

اللغة	التسمية	الوصف	أسماء أخرى
العربية	لم تُضف التسمية	لا يوجد وصف
الإنجليزية	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

بيانات

Wikidata item ^{الإنجليزية}

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