Congenital lobar emphysema

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Congenital lobar emphysema

ORPHA:1928Morphological anomaly

Also called Congenital lobar hyperinflation · Infantile lobar hyperinflation

What it is

A respiratory abnormality characterized by respiratory distress due to hyperinflation of one or more affected lobes of the lung.

Key facts

Prevalence
1-9 / 100 000
Age of onset
Adult, Childhood, Infancy, Neonatal
Inheritance
Not applicable
Classified as
Morphological anomaly

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

ICD-10 codes

Q33.8filed under a broader ICD-10 category — shared with 1 other rare disease

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Cross-references

GARD 2104MEDDRA 10010456MESH C535735MONDO 0007536OMIM 130710UMLS C0265797

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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