ORPHA:275938
Hemolytic disease due to fetomaternal alloimmunization
Synonyms: HDFN · Hemolytic disease of the fetus and newborn
- 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 | Hemolytic disease due to fetomaternal alloimmunization | HDFN · Hemolytic disease of the fetus and newborn |
| fr | Maladie hémolytique par allo-immunisation foetomaternelle | HDFN · Maladie hémolytique du foetus et du nouveau-né |
| de | Hämolytische Krankheit durch fetomaternale Alloimmunisierung | HDFN · Hämolytische Krankheit des Fetus und Neugeborenen |
| es | Enfermedad hemolítica por aloinmunización materno-fetal | Enfermedad hemolítica del feto y del recién nacido · HDFN |
| it | Malattia emolitica da alloimmunizzazione fetomaterna | |
| nl | Hemolytische ziekte door foetomaternale allo-immunisatie | HDFN · Hemolytische ziekte van foetus en neonaat |
| pt | Doença hemolítica por alo-imunização feto-materna | |
| pl | Choroba hemolityczna z powodu alloimmunizacji płodowo-matczynej | = en |
| cs | Hemolytická nemoc způsobená fetomaternální aloimunizací | = en |
| uk | Гемолітична хвороба внаслідок алоімунізації плода та матері | HDFN · Гемолітична хвороба плода та новонародженого |
| zh | 胎儿母体同种异体免疫所致溶血病 | 胎儿和新生儿溶血病 |
| tr | Fetomaternal alloimmünizasyona bağlı hemolitik hastalık | HDFN · Fetüs ve yenidoğanın hemolitik hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17163 | 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 (1):
- ORPHA:182047Rare acquired hemolytic anemia
rare hematological diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/275938
- This record as JSON: /data/d/275938.json