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Term ID: | 899 |
Name: | Arthritis, Psoriatic |
Definition: | A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. |
Alternative IDs: | OMIM:607507 |
ParentIDs: | MESH:D001168|MESH:D011565|MESH:D025242 |
TreeNumbers: | C05.116.900.853.625.800.424 |C05.550.114.145 |C05.550.114.865.800.424 |C17.800.859.675.175 |
Synonyms: | Arthritic Psoriasis |Arthropathies, Psoriatic |Arthropathy, Psoriatic |PSORAS1 |Psoriasis, Arthritic |Psoriasis Arthropathica |Psoriatic Arthritis |PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO, 1 |Psoriatic Arthropathies |Psoriati |
Slim Mappings: | Musculoskeletal disease|Skin disease |
Reference: |
MedGen: D015535
MeSH: D015535
OMIM: 607507;
Genes: LTA; NOD2; | Phenotypes | | Disease Causing ClinVar Variants | Variation_Name | GeneID | GeneSymbol | ClinicalSignificance | dbSNP | RCVaccession | TestedInGTR | PhenotypeIDs | Chromosome | Start | Stop | HGVS_c | HGVS_p | HGVS_g | OtherIDs | Disease_ClinVar | Disease_hgmd | NM_001159740.2(LTA):c.-9-198A>G | 4049 | LTA | risk factor | 909253 | RCV000015456; RCV000015457; | N | MedGen:C0027051,SNOMED CT:22298006; MedGen:C1835223,OMIM:607507 | 6 | 31540313 | 31540313 | NM_001159740.2:c.-9-198A>G | | NC_000006.11:g.31540313A>G | OMIM Allelic Variant:153440.0002 | C0027051 Myocardial infarction; C1835223 607507 Psoriatic arthritis, susceptibility to | | |
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