Rare diseases · Sign or symptom
Chronic lung disease
HP:0006528
What it means
According to the definitions of the American and British Thoracic Societies, including pulmonary functional tests, X-rays, and CT scans for items such as fibrosis, bronchiectasis, bullae, emphysema, nodular or lymphomatous abnormalities.
Rare diseases that can present with this16
Very common80–99%
2Common30–79%
7Sometimes5–29%
6- CTCF-related neurodevelopmental disorder
- Familial papillary or follicular thyroid carcinoma
- Familial papillary thyroid carcinoma with renal papillary neoplasia
- Joubert syndrome with Jeune asphyxiating thoracic dystrophy
- Neonatal acute respiratory distress syndrome due to SP-B deficiency
- Severe acute respiratory syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
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Start free with EleplanThis 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.