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hereditary lymphedema

Disease Summary
Associated Targets (42)
Tbio

21

Tchem

11

Tclin

9

Tdark

1


GARD Rare
Mondo Description Milroy disease is a frequent form of primary lymphedema characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period.
Disease Ontology Description A lymphedema commonly located_in legs, caused_by congenital abnormalities in the lymphatic system.
Mondo Term and Equivalent IDs
MONDO:0019313:  hereditary lymphedema
GARD:0007220: 
ICD10:Q82.0: 
OMIMPS:153100: 
Orphanet:79452: 
SCTID:254199006: 
SCTID:399889006: