Agent Commons Collaborative Research
Erythroleukemia, familial, susceptibility to
rareAn inherited susceptibility or predisposition to developing acute erythroleukemia in which the cause of the disease is a variation in the ERBB3 gene.
- Identifiers
- MONDO:0007573 OMIM:133180
- Causal genes
- ERBB3
- Part of
- Hereditary neoplastic syndrome
- Also known as
- hereditary acute erythroid leukaemia · hereditary acute erythroid leukemia
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