SPDA2
MCID: SPN226
MIFTS: 15

Spondyloarthropathy 2 (SPDA2)

Categories: Bone diseases, Eye diseases, Genetic diseases, Immune diseases, Muscle diseases, Rare diseases, Respiratory diseases

Aliases & Classifications for Spondyloarthropathy 2

MalaCards integrated aliases for Spondyloarthropathy 2:

Name: Spondyloarthropathy 2 57
Spondyloarthropathy, Susceptibility to, 2 57 13 70
Spda2 57

Characteristics:

OMIM®:

57 (Updated 05-Apr-2021)
Inheritance:
autosomal dominant


HPO:

31
spondyloarthropathy 2:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM® 57 183840
OMIM Phenotypic Series 57 PS106300
MedGen 41 C1866738
SNOMED-CT via HPO 68 263681008 399269003
UMLS 70 C1866738

Summaries for Spondyloarthropathy 2

MalaCards based summary : Spondyloarthropathy 2, also known as spondyloarthropathy, susceptibility to, 2, is related to spondyloarthropathy. An important gene associated with Spondyloarthropathy 2 is SPDA2 (Spondyloarthropathy, Susceptibility To, 2). Related phenotypes are abnormality of metabolism/homeostasis and abnormal joint morphology

More information from OMIM: 183840 PS106300

Related Diseases for Spondyloarthropathy 2

Diseases in the Spondyloarthropathy family:

Spondyloarthropathy 1 Spondyloarthropathy 2
Spondyloarthropathy 3 Juvenile Spondyloarthropathy

Diseases related to Spondyloarthropathy 2 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 spondyloarthropathy 11.0

Symptoms & Phenotypes for Spondyloarthropathy 2

Human phenotypes related to Spondyloarthropathy 2:

31
# Description HPO Frequency HPO Source Accession
1 abnormality of metabolism/homeostasis 31 HP:0001939
2 abnormal joint morphology 31 HP:0001367

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Apr-2021)
Joints:
spondyloarthropathy

Lab:
rheumatoid serologic tests negative

Clinical features from OMIM®:

183840 (Updated 05-Apr-2021)

Drugs & Therapeutics for Spondyloarthropathy 2

Search Clinical Trials , NIH Clinical Center for Spondyloarthropathy 2

Genetic Tests for Spondyloarthropathy 2

Anatomical Context for Spondyloarthropathy 2

Publications for Spondyloarthropathy 2

Articles related to Spondyloarthropathy 2:

# Title Authors PMID Year
1
Significant linkage to spondyloarthropathy on 9q31-34. 57
15234954 2004
2
Magnetic resonance imaging of the hand for the diagnosis of rheumatoid arthritis in the absence of anti-cyclic citrullinated peptide antibodies: a prospective study. 61
16832852 2006
3
Clinical analysis of 21 patients with psoriasis arthropathy. 61
15906536 2005
4
Validity and reliability of the EQ-5D self-report questionnaire in Chinese-speaking patients with rheumatic diseases in Singapore. 61
14626802 2003
5
Safety of anthrax vaccine: a review by the Anthrax Vaccine Expert Committee (AVEC) of adverse events reported to the Vaccine Adverse Event Reporting System (VAERS). 61
12051118 2002
6
The changing face of familial Mediterranean fever. 61
8989806 1996
7
Administration of methylprednisolone pulse in chronic arthritis in children. 61
2060171 1991

Variations for Spondyloarthropathy 2

Expression for Spondyloarthropathy 2

Search GEO for disease gene expression data for Spondyloarthropathy 2.

Pathways for Spondyloarthropathy 2

GO Terms for Spondyloarthropathy 2

Sources for Spondyloarthropathy 2

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-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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