ORPHA:238536
Congenital secondary erythrocytosis
Synonyms: Congenital secondary polycythemia
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Autosomal dominant, Autosomal recessive
- Age of onset
- Infancy, Neonatal
- 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 | Congenital secondary erythrocytosis | Congenital secondary polycythemia |
| fr | Erythrocytose secondaire congénitale | Polycythémie secondaire congénitale · Polyglobulie secondaire congénitale |
| de | Polyzythämie, sekundäre, kongenitale Form | Erythrozytose, sekundäre, kongenitale Form |
| es | Eritrocitosis secundaria congénita | Policitemia secundaria congénita |
| it | Eritrocitosi secondaria congenita | Policitemia secondaria congenita |
| nl | Congenitale secundaire erytrocytose | Congenitale secundaire polycytemie |
| pt | Policitemia secundária congénita | |
| pl | Wrodzona wtórna policytemia | Wrodzona wtórna nadkrwistość |
| cs | Vrozená sekundární polycytemie | Vrozená sekundární erytrocytóza |
| uk | Вроджена вторинна поліцитемія | Вроджений вторинний еритроцитоз |
| zh | 先天性继发性红细胞增多症 | 先天性继发性红细胞增多症 |
| tr | Doğumsal sekonder polisitemi | Doğumsal sekonder eritrositoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016540 | E | validated | |
| MONDO | 16540 | E | validated | |
| UMLS | C5679848 | E | validated |
E 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 (2):
- ORPHA:98427Erythrocytosis
rare hematological diseases - ORPHA:250165Genetic polycythemia
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/238536
- This record as JSON: /data/d/238536.json