JSON

mixed connective tissue disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0005854

Mixed connective tissue disease (MCTD) is a rare autoimmune disorder that is characterized by features commonly seen in three different connective tissue disorders: systemic lupus erythematosus, scleroderma, and polymyositis. Some affected people may also have symptoms of rheumatoid arthritis. Although MCTD can affect people of all ages, it appears to be most common in women under age 30. Signs and symptoms vary but may include Raynaud's phenomenon ; arthritis; heart, lung and skin abnormalities; kidney disease; muscle weakness, and dysfunction of the esophagus. The cause of MCTD is currently unknown. There is no cure but certain medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids and immunosuppresivedrugsmay help manage the symptoms. [ https://rarediseases.info.nih.gov/diseases/7051/mixed-connective-tissue-disease ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:0007051 (MONDO:equivalentTo)
  • DOID:3492 (MONDO:equivalentTo)
  • MESH:D008947 (Orphanet:809)
  • SCTID:398049005 (MONDO:equivalentTo)
  • UMLS:C0026272 (Orphanet:809)
  • NCIT:C84892 (MONDO:equivalentTo)
  • MedDRA:10027754 (Orphanet:809)
  • ICD10:M35.1 (Orphanet:809)
  • EFO:0007374 (MONDO:equivalentTo)
  • Orphanet:809 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
MCTD [ Orphanet:809 ]

closeMatch

http://identifiers.org/snomedct/33110008

http://identifiers.org/snomedct/398021003

definition

Mixed connective tissue disease (MCTD) is a rare autoimmune disorder that is characterized by features commonly seen in three different connective tissue disorders: systemic lupus erythematosus, scleroderma, and polymyositis. Some affected people may also have symptoms of rheumatoid arthritis. Although MCTD can affect people of all ages, it appears to be most common in women under age 30. Signs and symptoms vary but may include Raynaud's phenomenon ; arthritis; heart, lung and skin abnormalities; kidney disease; muscle weakness, and dysfunction of the esophagus. The cause of MCTD is currently unknown. There is no cure but certain medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids and immunosuppresivedrugsmay help manage the symptoms.

exactMatch

http://identifiers.org/meddra/10027754

http://identifiers.org/snomedct/398049005

http://linkedlifedata.com/resource/umls/id/C0026272

http://purl.obolibrary.org/obo/NCIT_C84892

http://www.orpha.net/ORDO/Orphanet_809

http://identifiers.org/mesh/D008947

http://purl.obolibrary.org/obo/DOID_3492

has exact synonym

sharp syndrome

MCTD

connective tissue disease overlap syndrome

mixed collagen vascular disease

id

MONDO:0005854

seeAlso

https://rarediseases.info.nih.gov/diseases/7051/mixed-connective-tissue-disease