WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0070212 hereditary lymphedema I 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.

1 Ontology

Name
Disease Ontology

7 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:2914 immune system disease A disease of anatomical entity that is located_in the immune system.
DOID:75 lymphatic system disease An immune system disease that is located_in the lymphatic system.
DOID:4977 lymphedema  
DOID:0050580 hereditary lymphedema A lymphedema commonly located_in legs, caused_by congenital abnormalities in the lymphatic system.
DOID:0070212 hereditary lymphedema I A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.

6 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050580 DOID:0070212
is_a DOID:75 DOID:0070212
is_a DOID:4 DOID:0070212
is_a DOID:2914 DOID:0070212
is_a DOID:4977 DOID:0070212
is_a DOID:7 DOID:0070212

6 Synonyms

Name Type
congenital primary lymphedema synonym
hereditary lymphedema type I synonym
LMPH1 synonym
Milroy disease synonym
Nonne-Milroy lymphedema synonym
PCL synonym