Rare diseases · Sign or symptom

Acute promyelocytic leukemia

HP:0004836

What it means

A type of acute myeloid leukemia in which abnormal promyelocytes predominate.

Rare diseases that can present with this1

The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.

Part of the broader category

Also called: Acute promyelocytic leukaemia

Acute promyelocytic leukemia

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This page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.