ORPHA:324924
Hereditary periodic fever syndrome
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hereditary periodic fever syndrome | |
| fr | Syndrome de fièvre récurrente héréditaire | Syndrome de fièvre périodique héréditaire |
| de | Hereditäres periodisches Fiebersyndrom | |
| es | Síndrome de fiebre periódica hereditaria | |
| it | Sindrome da febbre ricorrente ereditaria | |
| nl | Erfelijke periodieke koorts-syndroom | |
| pt | Síndrome da febre periódica hereditária | |
| pl | Dziedziczny zespół gorączki okresowej | |
| cs | Hereditární syndrom periodických horeček | |
| uk | Спадковий синдром періодичної лихоманки | |
| zh | 遗传性周期性发热综合征 | |
| tr | Kalıtsal periyodik ateş sendromu |
2
Cross-references
qualifier = Orphanet mapping relationE exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (3):
- ORPHA:101995Periodic fever syndrome
rare systemic and rheumatological diseases - ORPHA:324939Periodic fever syndrome of childhood
rare systemic or rheumatologic diseases of childhood - ORPHA:619238Rare hereditary autoinflammatory disease
rare genetic diseases
Children (11):
- ORPHA:566067CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome
- ORPHA:617919F12-associated cold autoinflammatory syndrome
- ORPHA:342Familial Mediterranean fever
- ORPHA:500062Infantile-onset periodic fever-panniculitis-dermatosis syndrome
- ORPHA:309025Mevalonate kinase deficiency
- ORPHA:576349NLRC4-related familial cold autoinflammatory syndrome
- ORPHA:247868NLRP12-associated hereditary periodic fever syndrome
- ORPHA:208650NLRP3-associated autoinflammatory disease
- ORPHA:652522Periodic fever-immunodeficiency-thrombocytopenia syndrome
- ORPHA:436166Periodic fever-infantile enterocolitis-autoinflammatory syndrome
- ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndrome
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/324924
- This record as JSON: /data/d/324924.json