Orphanet: Milroy disease

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Milroy disease

Disease definition

Milroy disease is a frequent form of primary lymphedema (see this term) characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period.

ORPHA:79452

Classification level: Disorder

Synonym(s):
- Hereditary lymphedema type I
- Nonne-Milroy lymphedema
Prevalence: Unknown
Inheritance: Autosomal dominant
Age of onset: Infancy, Neonatal
ICD-10: Q82.0
OMIM: 153100 247440 611944 613480 615907
UMLS: C1704423
MeSH: -
GARD: 7220
MedDRA: -

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Milroy disease

ORPHA:79452

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