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Spondylarthropathies (CUI C0949691) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0949691

Semantic Type: Disease or Syndrome

RADLEX Definition: Heterogeneous group of arthritic diseases sharing clinical and radiologic features and presence of the hla-B27 antigen. [MeSH]

CSP Definition: group of related inflammatory, arthritic diseases of the joints in the spine sharing clinical and radiologic features and are associated with the MHC class I molecule HLA-B27 antigen.

MSH Definition: Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others.

Synonyms & Abbreviations: (see Synonym Details)
Bechterew syndrome
Disorder of joint of spine (disorder)
Disorder of joint of spine
Marie Strumpell Spondylitis
Marie-Strumpell spondylitis
Spondarthropathy
Spondylarthropathies [Disease/Finding]
Spondylarthropathies
Spondylarthropathie
spondylarthropathy
Spondylarthrosis NOS
spondylarthrosis
Spondylitis, Marie-Strumpell
Spondyloarthropathies
spondyloarthropathy
Spondyloarthrosis
Syndrome, Bechterew

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN coordinate with specific vertebra MSH
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CTV3ID XUVpn SNOMEDCT_US
DATE_CREATED 2015-01-09T00:02:00 GARD
DATE_LAST_MODIFIED 2015-01-09T00:02:00 GARD
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DID 5006-0035 CSP
DISEASE_IDENTIFIER_ID 28957 GARD
DISEASE_IDENTIFIER_ID 28958 GARD
DX 20020101 MSH
EFFECTIVE_TIME 20020731 SNOMEDCT_US
HAS_GARD_PAGE true GARD
HN 2002 MSH
IDENTIFIER_SOURCE OMI GARD
IDENTIFIER_SOURCE Orp GARD
IDENTIFIER_TYPE_ID 1 GARD
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
MDA 20010803 MSH
MESH_DEFINITION Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others. NDFRT
MESH_DUI D025242 NDFRT
MESH_NAME Spondylarthropathies NDFRT
MESH_UI M0374011 NDFRT
MMR 20120703 MSH
MN C05.116.900.853.625.800 MSH
MN C05.550.114.865.800 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000010934 NDFRT
PM 2002 MSH
PRIMARY_PATH 10051265$10052775$10023213$10028395$Spondyloarthropathy$Spondyloarthropathies$Joint disorders$Musculoskeletal and connective tissue disorders MDR
PRIMARY_SOC 10028395 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/4971/spondylarthropathy/resources/1 GARD
RXAUI 3239919 RXNORM
RXAUI 3239920 RXNORM
RXAUI 3239921 RXNORM
RXAUI 5038849 RXNORM
RXAUI 5039626 RXNORM
RXAUI 5039971 RXNORM
RXCUI 1022545 RXNORM
SMQ_TERM_ADDVERSION 16.1 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 16.1 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 372109003 NDFRT
SNOMEDID D1-00137 SNOMEDCT_US
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS M53.99 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~M53.99 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS M53.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~M53.9 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUVpn SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~D1-00137 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T430250 MSH
TERMUI T430251 MSH
TERMUI T812516 MSH
TERMUI T812517 MSH
TERMUI T812518 MSH
TH NLM (2002) MSH
TH OMIM (2013) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0949691

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