ORPHA:717871
Rare systemic or rheumatologic disease with inflammatory bowel disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare systemic or rheumatologic disease with inflammatory bowel disease | |
| fr | Maladie systémique ou rhumatologique rare avec maladie inflammatoire de l'intestin | |
| de | Seltene systemische oder rheumatologische Krankheit mit entzündlicher Darmerkrankung | |
| es | Enfermedad sistémica o reumatológica rara con enfermedad inflamatoria intestinal | |
| it | Malattia sistemica o reumatologica rara con malattia infiammatoria dell'intestino | |
| nl | Zeldzame systemische of reumatologische ziekte met inflammatoire darmziekte | |
| pt | Rare systemic or rheumatologic diseases with inflammatory bowel disease | |
| pl | Rare systemic or rheumatologic disease with inflammatory bowel disease | |
| cs | Rare systemic or rheumatologic disease with inflammatory bowel disease |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:717862Rare disorder with inflammatory bowel disease
rare gastroenterological diseases; rare genetic diseases; rare transplant-related disorders
Children (7):
- ORPHA:404553Deficiency of adenosine deaminase 2
- ORPHA:674762Early-onset autoinflammatory syndrome due to A20 haploinsufficiency
- ORPHA:60030Loeys-Dietz syndrome
- ORPHA:699605NEMO deleted exon 5 autoinflammatory syndrome
- ORPHA:619363NOCARH syndrome
- ORPHA:436166Periodic fever-infantile enterocolitis-autoinflammatory syndrome
- ORPHA:85414Systemic-onset juvenile idiopathic arthritis
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/717871
- This record as JSON: /data/d/717871.json