ORPHA:182043
Rare constitutional hemolytic anemia
- 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 | Rare constitutional hemolytic anemia | |
| fr | Anémie hémolytique constitutionnelle rare | |
| de | Hämolytische Anämie, konstitutionelle, seltene | |
| es | Anemia hemolítica constitucional rara | |
| it | Anemia emolitica costituzionale rara | |
| nl | Zeldzame constitutionele hemolytische anemie | |
| pt | Anemia hemolítica constitucional rara | |
| pl | Rzadka konstytucjonalna niedokrwistość hemolityczna | |
| cs | Vzácné konstituční hemolytické anémie | |
| uk | Рідкісна конституціональна гемолітична анемія | |
| zh | 罕见全身性溶血性贫血 | |
| tr | Nadir yapısal hemolitik anemi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15910 | E | validated | |
| UMLS | C5680605 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:183651Rare constitutional anemia
rare genetic diseases - ORPHA:98363Rare hemolytic anemia
rare hematological diseases
Children (8):
- ORPHA:86818Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
- ORPHA:727394Autosomal recessive KLF1-related severe anemia
- ORPHA:79293Familial LCAT deficiency
- ORPHA:576742Genetic hemolytic uremic syndrome
- ORPHA:1046Lethal hemolytic anemia-genital anomalies syndrome
- ORPHA:688581Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome
- ORPHA:98364Rare constitutional hemolytic anemia due to a red cell membrane anomaly
- ORPHA:98369Rare constitutional hemolytic anemia due to an enzyme disorder
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/182043
- This record as JSON: /data/d/182043.json