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Inherited prekallikrein deficiency
rareAn instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0012901 OMIM:612423Orphanet:749
- Causal genes
- KLKB1
- Part of
- Coagulation protein diseaseHemorrhagic diseaseInherited blood coagulation disorderPrekallikrein deficiency
- Also known as
- congenital prekallikrein deficiency · fletcher factor (prekallikrein) deficiency · hereditary prekallikrein deficiency · prekallikrein deficiency, congenital
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