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Kidney Tissue Atlas Ontology
Last uploaded:
March 16, 2024
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Id | http://purl.obolibrary.org/obo/MONDO_0019313
http://purl.obolibrary.org/obo/MONDO_0019313
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Preferred Name | hereditary lymphedema |
Definitions |
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.
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Synonyms |
Nonne-Milroy syndrome
early onset lymphedema
Nonne’s syndrome
congenital hereditary lymphedema
hereditary lymphedema 1
Nonne-Milroy disease
Milroy's disease
congenital primary lymphedema
Nonne-Milroy lymphedema
hereditary lymphedema type I
hereditary lymphedema
lymphedema, hereditary
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
label |
hereditary lymphedema
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prefLabel |
hereditary lymphedema
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exactMatch | |
database_cross_reference |
ICD10:Q82.0
Orphanet:79452
GARD:0007220
SCTID:254199006
OMIMPS:153100
DOID:0050580
SCTID:399889006
ICD9:757.0
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notation |
MONDO:0019313
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in_subset | |
has related synonym |
Nonne-Milroy syndrome
early onset lymphedema
Nonne’s syndrome
congenital hereditary lymphedema
hereditary lymphedema 1
Nonne-Milroy disease
See more
See less
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id |
MONDO:0019313
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should_conform_to | |
textual 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.
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subClassOf | |
imported from | |
closeMatch | |
type | |
conformsTo | |
has exact synonym |
Milroy's disease
congenital primary lymphedema
Nonne-Milroy lymphedema
hereditary lymphedema type I
hereditary lymphedema
lymphedema, hereditary
See more
See less
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