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DO Term : hereditary lymphedema I [DOID:0070212] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.

synonyms:
ORDO:79452,
SNOMEDCT_US_2023_03_01:268355000,
GARD:7220,
NCI:C48829,
congenital primary lymphedema,
LMPH1,
ICD10CM:Q82.0,
PCL,
Milroy disease,
UMLS_CUI:C1704423,
MESH:D008209,
hereditary lymphedema type I,
Nonne-Milroy lymphedema

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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