OBO ID: DOID:0070213
Term Name: hereditary lymphedema II Search Ontology:
Synonyms:
  • late-onset lymphedema
  • LMPH2
  • lymphedema preacox
  • Meige disease
  • Meige lymphedema
Definition: A hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance. https://www.ncbi.nlm.nih.gov/pubmed/6342849
References:
  • GARD:3324
  • ICD10CM:I89.0
  • MESH:C562467
  • OMIM:153200
  • ORDO:90186
  • SNOMEDCT_US_2023_03_01:234098006
  • SNOMEDCT_US_2023_03_01:400040008
  • UMLS_CUI:C0238261
  • UMLS_CUI:C1704424
Ontology: Human Disease   ( DOID:0070213 )
Relationships
is a type of:
OTHER hereditary lymphedema II PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.