Milroy disease is a frequent form of primary lymphedema characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period. [ Orphanet:79452 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:79452 (MONDO:equivalentTo)
  • ICD10:Q82.0 (Orphanet:79452)
  • ICD9:757.0 (DOID:0050580)
  • SCTID:399889006 (MONDO:equivalentTo)
  • GARD:0007220 (Orphanet-shared)
  • OMIMPS:153100 (MONDO:equivalentTo)
  • DOID:0050580 (MONDO:equivalentTo)
  • SCTID:254199006 (MONDO:equivalentTo)
Subsets

ordo_disease

closeMatch

http://linkedlifedata.com/resource/umls/id/C1313885

http://identifiers.org/snomedct/75127007

http://identifiers.org/snomedct/205543002

http://identifiers.org/snomedct/205542007

http://identifiers.org/snomedct/205546005

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

definition

Milroy disease is a frequent form of primary lymphedema characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period.

exactMatch

http://identifiers.org/snomedct/254199006

http://linkedlifedata.com/resource/umls/id/C1704423

http://identifiers.org/snomedct/399889006

http://purl.obolibrary.org/obo/DOID_0050580

http://www.orpha.net/ORDO/Orphanet_79452

has exact synonym

hereditary lymphedema

hereditary lymphedema type I

Nonne-Milroy lymphedema

congenital primary lymphedema

lymphedema, hereditary

Milroy's disease

has related synonym

early onset lymphedema

Nonne’s syndrome

hereditary lymphedema 1

congenital hereditary lymphedema

Nonne-Milroy disease

Nonne-Milroy syndrome

id

MONDO:0019313

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml

Term relations