Search Ontology:
Human Disease

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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models