Transient erythroblastopenia of childhood
Synonyms: Transient acquired pure red cell aplasia
- Type
- Disease
- Group
- Disorder
- Age of onset
- Childhood, Infancy
- Status
- active
A rare, benign, red cell aplasia of young children or infants characterized by a normocytic normochromic anaemia with severe reticulocytopenia in otherwise normocellular bone marrow, and a complete spontaneous recovery within 1-2 months after diagnosis. Neutropenia and thrombocytosis may be associated findings at diagnosis, and a history of a preceding viral illness is frequent. No organomegaly is observed.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Transient erythroblastopenia of childhood | Transient acquired pure red cell aplasia |
| fr | Erythroblastopénie transitoire de l'enfance | Aplasie transitoire acquise de la lignée rouge |
| de | Erythroblastopenie, transiente, des Kindesalters | Erythroblastopenie, erworbene transiente |
| es | Eritroblastopenia transitoria de la infancia | Aplasia de glóbulos rojos pura adquirida transitoria |
| it | Eritroblastopenia transitoria dell'infanzia | Aplasia pura acquisita transitoria degli eritrociti |
| nl | Transiënte erytroblastopenie in de kindertijd | Transiënte verworven zuiver erytrocytaire aplasie |
| pt | Eritroblastopenia da infância, transitória | |
| pl | Przejściowa erytroblastopenia dziecięca | Przejściowa nabyta aplazja czysto czerwonokrwinkowa |
| cs | Tranzientní erytroblastopenie dětského věku | Tranzientní získaná čistá aplázie červené řady |
| uk | Транзиторна еритробластопенія дитячого віку | Транзиторна набута чиста еритроцитарна аплазія |
| zh | 儿童期短暂性幼红细胞减少症 | 暂时获得性纯红细胞再生障碍 |
| tr | Çocuklukta geçici eritroblastopeni | Geçici edinsel saf kırmızı hücre aplazisi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 227050 | E | validated | |
| ICD-10 | D60.1 | E | specific | validated |
| ICD-11 | 3A61.0 | NTBT | index | validated |
| MONDO | 0009197 | E | validated | |
| MeSH | C536980 | E | validated | |
| UMLS | C0238478 | E | validated | |
| GARD | 7793 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98421Primary acquired red cell aplasia
rare hematological diseases; rare transplant-related disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98871
- This record as JSON: /data/d/98871.json