Pelger-Huet-like anomaly and episodic fever with abdominal pain

MONDO:0009842

An autoinflammatory disease with defective neutrophil function caused by a homozygous Arg219His mutation in the transcription factor C/EBPε.

Also known as: Pelger-Huet-like anomaly and episodic fever with abdominal pain, immunodeficiency 108 with autoinflammation

10 clinical trials for this condition and its sub-types, 0 tagged with Pelger-Huet-like anomaly and episodic fever with abdominal pain itself.

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