FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary lymphedema I ID (Ontology) DOID:0070212 (Human Disease)
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.
Also Known As "congenital primary lymphedema" ; "hereditary lymphedema type I" ; "LMPH1" (for all, see Synonyms field below)
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  lymphedema
   |__hereditary lymphedema
       |__hereditary lymphedema I
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Synonyms
  • "congenital primary lymphedema" EXACT
    "hereditary lymphedema type I" EXACT
    "LMPH1" EXACT OMO:0003012
    "Milroy disease" EXACT
    "Nonne-Milroy lymphedema" EXACT
    "PCL" EXACT OMO:0003012
Secondary IDs
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GARD:7220
ICD10CM:Q82.0
MESH:D008209
NCI:C48829
ORDO:79452
SNOMEDCT_US_2023_03_01:268355000
UMLS_CUI:C1704423