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 [ https://rarediseases.info.nih.gov/diseases/7352/pemphigus ]

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Term information

database cross reference
  • SCTID:65172003 (MONDO:equivalentTo)
  • DOID:9182 (MONDO:equivalentTo)
  • NANDO:1200228 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C34909 (MONDO:equivalentTo)
  • Wikipedia:Pemphigus (EFO:1000749)
  • UMLS:C0030807 (MONDO:equivalentTo)
  • MESH:D010392 (MONDO:equivalentTo)
  • ICD9:694.4 (MONDO:i2s)
  • EFO:1000749 (MONDO:equivalentTo)
  • MEDGEN:45369 (MONDO:equivalentTo)
  • GARD:7352 (MONDO:GARD)
  • ICD10CM:L10 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare, nord_rare

exactMatch

http://identifiers.org/mesh/D010392

http://purl.obolibrary.org/obo/DOID_9182

http://identifiers.org/medgen/45369

http://purl.bioontology.org/ontology/ICD10CM/L10

http://identifiers.org/snomedct/65172003

http://linkedlifedata.com/resource/umls/id/C0030807

http://purl.obolibrary.org/obo/NCIT_C34909

id

MONDO:0006594

seeAlso

https://rarediseases.info.nih.gov/diseases/7352/pemphigus

Term relations