Structured Summary
Abstract
A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and Raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a speckled epidermal nuclear staining pattern on direct immunofluorescence.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
4 entry terms
- Connective Tissue Disease, Mixed
- MCTD
- Sharp Syndrome
- Syndrome, Sharp
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
a specific disease entity; do not confuse with CONNECTIVE TISSUE DISEASES
MeSH Record
History Note
79
MeSH Record
Previous Indexing
- Collagen Diseases (1972-1978)
- Lupus Erythematosus, Systemic (1972-1978)
- Scleroderma, Systemic (1972-1978)
MeSH Hierarchy
Tree Number
MeSH Record
NLM Classification
QZ 192
AMA Style
References
- National Library of Medicine. Mixed Connective Tissue Disease. Medical Subject Headings (MeSH). 2026. Unique ID D008947. http://id.nlm.nih.gov/mesh/2026/D008947
- Mixed Connective Tissue Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Mixed_connective_tissue_disease
- Mixed Connective Tissue Disease. In: Wikidata. https://www.wikidata.org/wiki/Q1622407