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Orphanet Rare Disease Ontology
Last uploaded:
December 4, 2024
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| Id | http://www.orpha.net/ORDO/Orphanet_318
http://www.orpha.net/ORDO/Orphanet_318
|
|---|---|
| Preferred Name | Acute erythroid leukemia |
| Definitions |
A rare unclassified acute myeloid leukemia characterized by a proliferation of immature cells exclusively of the erythroid lineage without a significant myeloblastic component. Microscopically, the cells may be undifferentiated or proerythroblastic in appearance. Patients may present with pancytopenia with fatigue, infections, and mucocutaneous bleedings, as well as weight loss, fever, and night sweats. Prognosis is poor.
|
| Synonyms |
AML M6
Acute myeloid leukemia M6
Erythroleukemia
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition_citation | Orphanet |
|---|---|
| definition | A rare unclassified acute myeloid leukemia characterized by a proliferation of immature cells exclusively of the erythroid lineage without a significant myeloblastic component. Microscopically, the cells may be undifferentiated or proerythroblastic in appearance. Patients may present with pancytopenia with fatigue, infections, and mucocutaneous bleedings, as well as weight loss, fever, and night sweats. Prognosis is poor. |
| label |
Acute erythroid leukemia
|
| prefLabel |
Acute erythroid leukemia
|
| hasDbXref |
MeSH:D004915
UMLS:C0023440
ICD-11:2A60.35
ICD-10:C94.0
OMIM:133180
|
| notation |
ORPHA:318
|
| alternative_term |
AML M6
Acute myeloid leukemia M6
Erythroleukemia
|
| present_in |
Worldwide AND has_annual_incidence_range : Unknown
Worldwide AND has_point_prevalence_range : Unknown
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| part_of | |
| prefixIRI |
ORDO:Orphanet_318
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| expertlink | |
| subClassOf | |
| type | |
| has_inheritance |
Not applicable
|
| has_age_of_onset |
Adolescent
Adult
Childhood
Elderly
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