FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary lymphedema II ID (Ontology) DOID:0070213 (Human Disease)
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.
Also Known As "late-onset lymphedema" ; "LMPH2" ; "lymphedema preacox" (for all, see Synonyms field below)
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
lymphedema                      |
 |__hereditary lymphedema_______|
                                hereditary lymphedema II
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Is a hereditary lymphedema
autosomal dominant disease
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Synonyms
  • "late-onset lymphedema" EXACT
    "LMPH2" EXACT OMO:0003012
    "lymphedema preacox" EXACT
    "Meige disease" EXACT
    "Meige lymphedema" EXACT
Secondary IDs
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GARD:3324
ICD10CM:I89.0
MESH:C562467
MIM:153200
ORDO:90186
SNOMEDCT_US_2023_03_01:234098006
SNOMEDCT_US_2023_03_01:400040008
UMLS_CUI:C0238261
UMLS_CUI:C1704424