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Inherited prekallikrein deficiency

MONDO:0012901

An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.

Also known as: congenital prekallikrein deficiency, fletcher factor (prekallikrein) deficiency, hereditary prekallikrein deficiency, Fletcher Factor deficiency, PKK deficiency, prekallikrein deficiency, prekallikrein deficiency, congenital

12 clinical trials for this condition and its sub-types, 0 tagged with Inherited prekallikrein deficiency itself.

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