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Cell Culture Ontology
Preferred Name | pemphigus | |
Synonyms |
pemphigus |
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Definitions |
Pemphigus is a group of chronic autoimmune skin diseases characterised by blisters formation on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterised, of which paraneoplastic pemphigus is extremely rare. [ Orphanet:63455 ] a rare group of blistering autoimmune diseases that affect the skin and mucous membranes. Pemphigus is a group of rare autoimmune diseases that cause blistering of the skin and mucous membranes (mouth, nose, throat, eyes, and genitals).This conditioncan occur at any age, but often strikes people in middle or older age. Studies have shown that some populations may be at greater risk for certain types of pemphigus. For instance, people of Jewish descent and those from India, Southeast Europe, and the Middle East are at greater risk for pemphigus vulargis, while pemphigus foliaceus is more common in North America, Turkey, and South America. Pemphigus is a chronic disease which is best controlled by early diagnosis and treatment.Treatment includes steroids to reduce inflammation,drugs that suppress the immune system responseand antibiotics to treat associated infections. There are four main types of pemphigus: Pemphigus vulgaris Pemphigus foliaceus IgA pemphigus Paraneoplastic pemphigus |
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ID |
http://www.ebi.ac.uk/efo/EFO_1000749 |
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database_cross_reference |
MedDRA:10034280 NCIt:C34909 UMLS:C0030807 NANDO:1200228 icd11.foundation:191659986 Wikipedia:Pemphigus MESH:D010392 SCTID:65172003 MONDO:0006594 ICD10CM:L10 MEDGEN:45369 NCIT:C34909 MeSH:D010392 DOID:9182 GARD:7352 ICD10:L10 ICD9:694.4
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definition |
Pemphigus is a group of chronic autoimmune skin diseases characterised by blisters formation on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterised, of which paraneoplastic pemphigus is extremely rare. [ Orphanet:63455 ] a rare group of blistering autoimmune diseases that affect the skin and mucous membranes. Pemphigus is a group of rare autoimmune diseases that cause blistering of the skin and mucous membranes (mouth, nose, throat, eyes, and genitals).This conditioncan occur at any age, but often strikes people in middle or older age. Studies have shown that some populations may be at greater risk for certain types of pemphigus. For instance, people of Jewish descent and those from India, Southeast Europe, and the Middle East are at greater risk for pemphigus vulargis, while pemphigus foliaceus is more common in North America, Turkey, and South America. Pemphigus is a chronic disease which is best controlled by early diagnosis and treatment.Treatment includes steroids to reduce inflammation,drugs that suppress the immune system responseand antibiotics to treat associated infections. There are four main types of pemphigus: Pemphigus vulgaris Pemphigus foliaceus IgA pemphigus Paraneoplastic pemphigus
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gwas_trait |
true
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has_exact_synonym |
pemphigus
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id |
EFO:1000749
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in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar |
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label |
pemphigus
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notation |
EFO:1000749
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preferred label |
pemphigus
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prefLabel |
pemphigus
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see also | ||
skos_exactMatch |
http://purl.bioontology.org/ontology/ICD10CM/L10 http://identifiers.org/mesh/D010392 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/191659986 http://linkedlifedata.com/resource/umls/id/C0030807 http://identifiers.org/snomedct/65172003 http://purl.obolibrary.org/obo/EFO_1000749 http://purl.obolibrary.org/obo/NCIT_C34909 |
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term editor |
Sirarat Sarntivijai
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subClassOf |
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