A rare acute myeloid leukemia that occurs predominantly in childhood and particularly in children with Down syndrome (DS-AMKL). Nonspecific symptoms may be irritability, weakness, and dizziness while specific symptoms include pallor, fever, mucocutaneous bleeding, hepatosplenomegaly, neurological manifestations and rarely lymphadenopathy. Acute panmyelosis with myelofibrosis may also be associated with AMKL. In contrast to DS-AMKL (around 80 % survival), non-DS-AMKL is an AML subgroup associated with poor prognosis.

Synonyms: AML M7 Acute myeloid leukemia M7 AMKL Acute megakaryocytic leukemia

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Term information

database cross reference
  • UMLS:C0023462 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:C94.2 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
hasDbXref

UMLS:C0023462

ICD-10:C94.2

notation

ORPHA:518