PedAM
Pediatric Disease Annotations & Medicines
| Disease | c1 inhibitor deficiency |
| Phenotype | C0019243|hereditary angio-oedema |
| Sentences | 1 |
| 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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