Belgian Genetic Tests database
Milroy disease
| Name: |
Milroy disease
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| Description: |
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.
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| ORPHAcode: |
79452
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| Synonyms: |
Hereditary lymphedema type I
Nonne-Milroy lymphedema
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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