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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease hereditary angioedema
Comorbidity C0019243|hereditary angio-oedema
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PubMedID- 22417938 hereditary angio-oedema due to c1 inhibitor deficiency (hae-c1-inh) is a rare inherited disorder characterised by recurring and debilitating episodes of cutaneous swelling and abdominal pain and less frequent episodes of laryngeal oedema.

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