Rare diseases · Sign or symptom

Unusual upper respiratory tract infection

HP:5210121

What it means

Increased susceptibility to infection of the upper respiratory tract, as manifested by recurrent or severe infection of the nose, sinuses, pharynx, larynx, or middle ear, or by infection caused by an atypical or opportunistic organism.

Recurrent or severe sinopulmonary infections are characteristic of humoral (B-cell) deficiencies, complement defects, and phagocyte disorders. This phenotype is also frequently observed in combined immunodeficiencies (e.g., DOCK8 deficiency) and hyper-IgE syndromes (e.g., STAT3 deficiency).

Part of the broader category

Unusual upper respiratory tract infection

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This page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.