Sneddon syndrome
form of arteriopathy
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Sneddon syndrome
Summary
Sneddon syndrome is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Sneddon syndrome's instance of is recorded as rare disease[3].
- Sneddon syndrome's instance of is recorded as class of disease[4].
- Sneddon syndrome is a type of artery disease[5].
- Sneddon syndrome is a type of vascular skin disease[6].
- Sneddon syndrome is a type of autoimmune skin disease[7].
- Sneddon syndrome is a type of autoimmune connective tissue disorder[8].
- Sneddon syndrome is a type of autoimmune disease of the nervous system[9].
- Sneddon syndrome is a type of genetic skin vascular disorder[10].
- Sneddon syndrome is a type of rare genetic immune disease[11].
- Sneddon syndrome is a type of genetic nervous system disorder[12].
- Sneddon syndrome is a type of central nervous system and retinal vascular disease[13].
- Sneddon syndrome is a type of other acquired skin disease[14].
- Sneddon syndrome is a type of genetic systemic or rheumatologic disease[15].
- Sneddon syndrome's health specialty is recorded as rheumatology[16].
- Sneddon syndrome's genetic association is recorded as ADA2[17].
- Sneddon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_13096[18].
- Sneddon syndrome's exact match is recorded as http://identifiers.org/doid/DOID:13096[19].
- Sneddon syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_820[20].
- Sneddon syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Sneddon syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[22]