hereditary lymphedema I

Term ID

DOID:0070212

Synonyms

• congenital primary lymphedema
• hereditary lymphedema type I
• LMPH1
• Milroy disease
• PCL

Definition

A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood. https://www.ncbi.nlm.nih.gov/pubmed/9817924

References

• GARD:7220
• ICD10CM:Q82.0
• MESH:D008209
• NCI:C48829
• ORDO:79452
• SNOMEDCT_US_2023_03_01:268355000
• UMLS_CUI:C1704423

Ontology

Human Disease   ( DOID:0070212 )