About: Primary lymphedema

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human disease

Attributes	Values
rdf:type	Item
description	Krankheit (de) Human disease (en) մարդու հիվանդություն (hy) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q7243149-056FAD25-447F-4329-9D4F-37ADFECC0950 wds:Q7243149-0AC218C3-4FA1-4027-9E64-D36B0DE7033F wds:Q7243149-F6560694-D3E7-4C4E-A19A-6322B8CF4424
exact match	http://www.orpha.net/ORDO/Orphanet_77240
ICD-10	wds:Q7243149-672A4B1F-8479-4950-8292-3020F8E4E83C
Mondo ID	wds:Q7243149-9D68D2F6-A031-4084-8F1B-96DA81FCDF6B
Disease Ontology ID	wds:Q7243149-DD1456D2-6E78-4EFB-A75B-FDDE33E65FF6
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0019175
ICD-10	Q82.0
Mondo ID	MONDO_0019175
rdfs:label	Nonne-Milroy-Meige-Syndrom (de) Primary lymphedema (en) lymphœdème primaire (fr) primarni limfedem (sl)
skos:prefLabel	Nonne-Milroy-Meige-Syndrom (de) Primary lymphedema (en) lymphœdème primaire (fr) primarni limfedem (sl)
name	Nonne-Milroy-Meige-Syndrom (de) Primary lymphedema (en) lymphœdème primaire (fr) primarni limfedem (sl)
instance of	wds:Q7243149-4E662273-1FCE-4D67-9404-078A2DD0C1A2
instance of	class of disease
subclass of	wds:Q7243149-2d7fa310-456d-482b-2ff5-fe3098e04780 wds:Q7243149-66BFE321-4577-4589-AEAF-1B7A8C20E39C
subclass of	hereditary lymphedema lymphatic system malformation
Encyclopædia Britannica Online ID	wds:Q7243149-B61696D6-CDE8-4D0B-9FCB-C28C730B982D
Encyclopædia Britannica Online ID	topic/primary-lymphedema
Orphanet ID	wds:Q7243149-af939a23-4f1a-fb05-77be-5aaf81f91497
ICD-10-CM	wds:Q7243149-C6E1EC4B-3DE1-4A3B-9B97-4378D41413C7
Orphanet ID	77240
ICD-10-CM	I89.0
Medical Dictionary...ory Activities ID	wds:Q7243149-23999CA6-52B4-4C7A-A14E-076A0AD76C40
ICD-9 ID	wds:Q7243149-1D8D78AA-8D93-4065-A048-BAD4AC71693B
Medical Dictionary...ory Activities ID	http://purl.bioontology.org/ontology/MDRFRE/10010535
Medical Dictionary...ory Activities ID	10010535
ICD-9 ID	757.0
skos:altLabel	Hereditary edema of legs (en) Hereditary edema of legs NOS (disorder) (en) Hereditary edema of legs [dup] (disorder) (en) Hereditary trophedema (disorder) (en) Hereditary trophoedeme (en) Primary Lymphedema (en) Troncular lymphatic malformation (en) hereditary trophedema (en) lymphœdème héréditaire (fr) obsolete hereditary trophedema (en)
NCI Thesaurus ID	wds:Q7243149-96AB11C8-183D-4D1F-BED0-898CD3532B38
UMLS CUI	wds:Q7243149-e9336641-45f6-5fb0-cce8-142e40d3db0d
on focus list of Wikimedia project	wds:Q7243149-CE6D372E-BB66-4587-B12D-48DB2FB52EA0
Microsoft Academic ID	wds:Q7243149-D62B679C-48F3-4D6D-992A-A575E2890E13
ICD-11 ID (MMS)	wds:Q7243149-83a669cd-3f91-47b7-bca5-fd1abeba3008
ICD-11 (foundation)	wds:Q7243149-0b7f67ff-413f-bec6-7c02-5b80a195782b
Microsoft Academic ID	https://makg.org/entity/2778437666
NCI Thesaurus ID	C48829
UMLS CUI	C0026147
on focus list of Wikimedia project	WikiProject Medicine
Microsoft Academic ID	2778437666
ICD-11 ID (MMS)	BD93.0
ICD-11 (foundation)	794588197
WikiProjectMed ID	wds:Q7243149-7866A420-E76A-45E9-A361-9E937D01098F
WikiProjectMed ID	Primary lymphedema
is owl:sameAs of	Primary lymphedema Primary lymphedema
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q7243149 Primary lymphedema https://de.wikipedia.org/wiki/Nonne-Milroy-Meige-Syndrom https://ar.wikipedia.org/wiki/%D9%88%D8%B0%D9%85%D8%A9_%D9%84%D9%85%D9%81%D9%8A%D8%A9_%D8%A3%D9%88%D9%84%D9%8A%D8%A9
is subclass of of	Lymphedema praecox microcephaly lymphoedema chorioretinal dysplasia hereditary lymphedema Meige lymphedema hypotrichosis–lymphedema–telangiectasia syndrome Lymphedema–distichiasis syndrome primary lymphedema with associated anomalies Lymphedema tarda
is subclass of of	wds:Q6839330-24ECCC62-DBDA-4575-B2F2-F1556EBE93C2 wds:Q3508768-c0a37ddd-4d2b-c115-7e9a-815d0f01174d wds:Q1996246-4e6738e2-4b86-5b5e-6468-a00a19bd55dc wds:Q16964430-895e49de-47f8-c641-0fd2-220ef19647b5 wds:Q110979258-4ba0b45a-43b8-f4e3-bdf6-2cc0a5c1e450 wds:Q6809999-6b083237-4e2d-99f1-db77-c3df28a8c9fd wds:Q55788282-344C226B-AE36-461A-A124-06C5186F245D wds:Q5961451-8aaa8afb-4dce-0ddf-70ab-92672efd4b11
is main subject of	The role of CT in the diagnosis of primary lymphedema of the lower limb Modified Charles procedure using negative pressure dressings for primary lymphedema: a functional assessment Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature Omental transposition in primary lymphedema Angiosarcoma in primary lymphedema of the lower extremity--Stewart-Treves syndrome Pleural effusion associated with primary lymphedema: a perspective on the yellow nail syndrome Lymphatic capillary pressure in patients with primary lymphedema Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene

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