Home
User Guide
What's in a MalaCard Search Guide Our Sources
Analysis Tools
GeneCards GeneAnalytics GeneAlaCart PathCards VarElect
News and Views Disease Lists/Categories
About
About MalaCards Datasets Our Publications Weizmann Institute LifeMap Discovery® Terms of Use MalaCards Team
SPDA3
MCID: SPN256
MIFTS: 11

Spondyloarthropathy 3 (SPDA3)

Categories: Bone diseases, Eye diseases, Genetic diseases, Immune diseases, Muscle diseases, Rare diseases, Respiratory diseases
Genes Publications
Sources

Aliases & Classifications for Spondyloarthropathy 3

About this section

MalaCards integrated aliases for Spondyloarthropathy 3:

Name: Spondyloarthropathy 3 57
Spondyloarthropathy, Susceptibility to, 3 57 13
Spda3 57

Classifications:

MalaCards categories:
Global: Genetic diseases Rare diseases
Anatomical: Bone diseases Immune diseases Eye diseases Respiratory diseases Muscle diseases
See all MalaCards categories (disease lists)


External Ids:

OMIM® 57 613238
OMIM Phenotypic Series 57 PS106300
Sources

Summaries for Spondyloarthropathy 3

About this section
MalaCards based summary : Spondyloarthropathy 3, is also known as spondyloarthropathy, susceptibility to, 3. An important gene associated with Spondyloarthropathy 3 is SPDA3 (Spondylarthropathy, Susceptibility To, 3).

More information from OMIM: 613238 PS106300
Sources

Related Diseases for Spondyloarthropathy 3

About this section

Diseases in the Spondyloarthropathy family:

Spondyloarthropathy 1 Spondyloarthropathy 2
Spondyloarthropathy 3 Juvenile Spondyloarthropathy

Sources

Symptoms & Phenotypes for Spondyloarthropathy 3

About this section

Clinical features from OMIM®:

613238 (Updated 05-Mar-2021)

Sources

Drugs & Therapeutics for Spondyloarthropathy 3

About this section

Search Clinical Trials , NIH Clinical Center for Spondyloarthropathy 3

Sources

Genetic Tests for Spondyloarthropathy 3

About this section
Sources

Anatomical Context for Spondyloarthropathy 3

About this section
Sources

Publications for Spondyloarthropathy 3

About this section

Articles related to Spondyloarthropathy 3:

# Title Authors PMID Year
1
Association of chromosome 2q36.1-36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families. 57
19416804 2009
2
The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis. 57
15309690 2004
3
Identification of major loci controlling clinical manifestations of ankylosing spondylitis. 57
12905477 2003
4
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci. 57
11231900 2001
5
Certain Autoimmune Manifestations Are Associated With Distinctive Karyotypes and Outcomes in Patients With Myelodysplastic Syndrome: A Retrospective Cohort Study. 61
27043672 2016
6
A T-cell-based enzyme-linked immunospot assay for tuberculosis screening in Chinese patients with rheumatic diseases receiving infliximab therapy. 61
21161670 2011
7
Malignancies in children who initially present with rheumatic complaints. 61
9880449 1999
Sources

Variations for Spondyloarthropathy 3

About this section
Sources

Expression for Spondyloarthropathy 3

About this section
Search GEO for disease gene expression data for Spondyloarthropathy 3.
Sources

Pathways for Spondyloarthropathy 3

About this section
Sources

GO Terms for Spondyloarthropathy 3

About this section
Sources

Sources for Spondyloarthropathy 3

About this section
3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Content
Loading form....