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Acute myeloid leukemia

disorder

SNOMED 91861009CUI C0023467

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Acute myeloid leukaemia

HP:0004808

Related Conditions

Acute myelofibrosis(child)

Acute promyelocytic leukaemia (clinical)(child)

Acute myelomonocytic leukaemia (clinical)(child)

Acute megakaryoblastic leukaemia(child)

Acute myeloid leukaemia, minimal differentiation, FAB M0(child)

Acute myeloid leukemia without maturation, FAB M1(child)

Acute myeloid leukemia with maturation, FAB M2(child)

Acute myeloid leukemia in remission(child)

Leukaemic infiltration of skin in acute myeloid leukaemia(child)

Basophilic leukemia(child)

Erythroleukaemia(child)

Acute myeloid leukaemia with multilineage dysplasia(child)

Core binding factor acute myeloid leukemia(child)

Cytogenetically normal acute myeloid leukaemia(child)

Inherited acute myeloid leukaemia(child)

Refractory AML (acute myelocytic leukemia)(child)

Relapsing AML (acute myelocytic leukemia)(child)

Acute myeloid leukaemia with NPM1 somatic mutation(child)

Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13)(child)

Acute myeloid leukaemia with CEBPA somatic mutations(child)

Quick Facts

SNOMED CT: 91861009
UMLS CUI: C0023467
Fully Specified Name: Acute myeloid leukemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1
Known Treatments: 20

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.