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inherited prekallikrein deficiency

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Mondo Description An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0012901:  inherited prekallikrein deficiency
GARD:0004477: 
MESH:C562725: 
Orphanet:749: