Rare lymphatic malformation

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Rare lymphatic malformation

ORPHA:2415Category

Also called LM · Lymphangioma

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Prevalence
1-5 / 10 000 (Europe)
Age of onset
Infancy, Neonatal
Inheritance
Not applicable
Classified as
Category

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.

ICD-10 codes

D18.1ICD-10 names this disease exactly — shared with 6 other rare diseases

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 9789MONDO 2013UMLS C5575909

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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