/hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

Rare Disease

MONDO:0015801

Patient-Friendly Information

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Primary Focus

RDCP:PAG0000016US

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inherited bleeding disorder, platelet-type

MONDO:0000009

factor XIII deficiency

MONDO:0002241

factor VII deficiency

MONDO:0002244

factor X deficiency

MONDO:0002247

purpura

MONDO:0002610

vascular hemostatic disease

MONDO:0003159