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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/106300
http://purl.bioontology.org/ontology/OMIM/106300
|
|---|---|
| Preferred Name | SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 |
| Synonyms |
ANKYLOSING SPONDYLITIS, SUSCEPTIBILITY TO
BECHTEREW SYNDROME
MARIE-STRUMPELL SPONDYLITIS
SPDA1
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
ANKYLOSING SPONDYLITIS, SUSCEPTIBILITY TO
BECHTEREW SYNDROME
MARIE-STRUMPELL SPONDYLITIS
SPDA1
|
|---|---|
| prefLabel | SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1
|
| Gene Symbol |
HLA-B
SPDA1
|
| Scope Statement | Overall prevalence is between 0.5 and 14 per 100,000 people per year [MISCELLANEOUS]
Spondyloarthropathy includes a spectrum of related disorders, including, 1 - ankylosing spondylitis (AS), 2 - a subset of psoriatic arthritis (PsA), 3 - reactive arthritis (ReA), 4 - arthritis associated with inflammatory bowel disease (AIBD), 5 - undifferentiated spondyloarthropathy (USpA) [MISCELLANEOUS]
Susceptibility conferred by mutation in the major histocompatibility complex, class I, B gene (HLA-B, 142830.0001) [MOLECULAR BASIS]
Genetic heterogeneity (see spondyloarthropathy, susceptibility to, 2 183840) [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T033
|
| Gene Locus | 6p21.3
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 106300
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1862852
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
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| Delete | Subject | Author | Type | Created |
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| No notes to display |