thromboangiitis obliterans
Human disease
Facts
14 properties- Instance of
- designated intractable/rare disease, class of disease[2]
- Subclass of
- peripheral vascular disease, predominantly medium-vessel vasculitis, secondary glomerular disease[4][5][6]
- Age of onset
- adult onset[15]
- Drug or therapy used for treatment
- tolazoline, isoxsuprine[13][14]
- Has phenotype
- sensory peripheral neuropathy, vasculitis, arterial thrombosis, gangrene, ulcer, acrocyanosis, arthralgia, paresthesia, intermittent claudication, Raynaud disease, Superficial thrombophlebitis, Acroparesthesia, insomnia, chronic arterial occlusive disease[17][18][19][20][21][22][23][24][25][26][27][28][29][30]
- Health specialty
- cardiology, rheumatology[11][12]
- ICD-9-CM
- 443.1[9]
- NCI Thesaurus ID
- C35070[10]
- Named after
- Leo Buerger[3]
- On focus list of Wikimedia project
- WikiProject Medicine[16]
- P14541
- 4fPWyb[31]
- P14914
- D36258[32]
- Prevalence
- +0.0003[8]
🏷️ Also known as
en Buerger disease
en thromboangiitis obliterans
en BUERGER DISEASE
en Presenile gangrene
en Buerger's disease
en Presenile gangrene (disorder)
en Thromboangiitis obliterans
en Thromboangiitis obliterans NOS (disorder)
en Thromboangiitis obliterans [Buerger's disease]
en Thromboangiitis obliterans (disorder)
ar Buerger's disease
ar مرض بورغر
cs Bürgerova choroba
da Buergers sygdom
da thromboangiitis obliterans
de Endarteriitis obliterans
de Winiwater-Buerger-Krankheit
de Thrombangiitis obliterans
de Endophlebitis obliterans
de Morbus Winiwarter-Buerger
🔖 Identifiers · 36
- Library of Congress authority ID
- sh85135068
- OpenAlex ID
- C2781265703
- Image (Wikimedia Commons)
- 55 year old female with advanced Buerger's disease.jpg ↗
- BNCF Thesaurus ID
- 43182
- Disease Ontology ID
- DOID:12918
- DiseasesDB
- 1762
- EMedicine ID
- 460027
- Encyclopaedia Beliana ID
- buergerova-choroba
- Encyclopædia Britannica Online ID
- science/Buergers-disease
- Encyclopædia Universalis ID
- maladie-de-buerger
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
Show all 36 identifiers +24
- Experimental Factor Ontology ID
- 1001211
- External data available at URL
- www.nanbyou.or.jp
- Freebase ID
- /m/044d8l
- GARD rare disease ID
- 5969
- ICD-10-CM
- I73.1
- ICD-11 ID (Foundation)
- 1000683110
- ICD-11 ID (MMS)
- 4A44.8
- JSTOR topic ID (archived)
- thromboangiitis-obliterans
- KEGG ID
- H01625
- Lex ID
- Buergers_sygdom
- MeSH descriptor ID
- D013919
- MeSH tree code
- C14.907.137.870, C14.907.940.905
- MedlinePlus ID
- 000172
- Mondo ID
- MONDO_0008889
- NL CR AUT ID
- ph920019
- National Library of Israel J9U ID
- 987007536586205171
- OMIM ID
- 211480
- Orphanet ID
- 36258
- Patientplus ID
- buergers-disease-pro
- PatientsLikeMe condition ID
- buerger-s-disease
- UMLS CUI
- C0040021
- WikiProjectMed ID
- Thromboangiitis obliterans
- WikiSkripta article ID
- 7096
- Yale LUX ID
- concept/99a2907f-83fe-47cb-bdb7-360bc8bb56a3
🔗 Connections
Drug or therapy used for treatment 2
Health specialty 2
← Medical condition treated 2
On focus list of Wikimedia project 1
Subclass of 1
Symptoms and signs 1
← Has cause 1
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Summary
thromboangiitis obliterans is a designated intractable/rare disease[1].