Test your own case

Run a real case through the WHO 2022 / ICC 2022 engine.

Enter the signals from a case you already know the answer to. The engine is deterministic and rule-based, so you can check it directly. Every call returns a signed, independently verifiable record. Research use only; decision support, not a diagnostic device.

Blast % (marrow)

Lineage

Molecular mutations

Comma separated. Recognized: NPM1, CEBPA-bZIP, TP53 (ICC entity), FLT3-ITD (risk flag), and the MR-defining genes ASXL1, BCOR, EZH2, SF3B1, SRSF2, STAG2, U2AF1, ZRSR2, RUNX1 (RUNX1 is MR under ICC only).

Fusions (cytogenetic / molecular)

Comma separated, using the A::B convention.

Karyotype (optional)

Descriptive only. Complex / adverse karyotype (e.g. -7, del(5q), ≥3 abnormalities) is not yet parsed for MR-cytogenetics; enter a defining rearrangement in the Fusions field instead.

Flow markers (optional)

Antecedent MDS / MDS-MPN Prior cytotoxic / radiation therapy

Enter a case and click Classify & sign. You will get the WHO 2022 and ICC 2022 calls, any diagnostic qualifiers, the rationale for each, and a signed record you can verify.

Research use only. The classification engine is deterministic WHO 2022 / ICC 2022 decision support, not a diagnostic device and not a diagnosis. Molecular and cytogenetic inputs are entered by you; Axiisium does not infer them here. Every output is a signed, tamper-evident record verifiable by anyone.