Leukemia, acute myeloid

Preferred Label : Leukemia, acute myeloid;

Symbol : AML;

CISMeF acronym : AML;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Leukemia, acute myelogenous;

Included titles and symbols : Leukemia, acute myeloid, susceptibility to;

Inheritance : Autosomal dominant; Somatic mutation;

Molecular basis : Caused by mutation in the alpha CCAAT/enhancer-binding protein (C/EBP) gene (CEBPA, 116897.0007);

Prefixed ID : #601626;

Details

Origin ID

601626;

UMLS CUI

C0023467;

Automatic exact mappings (from CISMeF team)
- Acute Myeloid Leukemia Pathway [NCIt concept]
- Acute myelogenous leukemia [PASCAL descriptor]
- Acute myeloid leukaemia, NOS [ICD-11 Extension code]
- Acute myeloid leukaemias and related precursor neoplasms [ICD-11 Category]
- Acute myeloid leukemia - category (morphologic abnormality) [SNOMED CT concept]
- Acute myeloid leukemia with recurrent genetic anomaly [ORDO Disease]
- Myeloid leukemia, subacute [MedDRA LLT]
- NCI CTEP SDC Acute Myeloid Leukemia Sub-Category Terminology [NCIt concept]
Currated CISMeF NLP mapping
- Acute Myeloid Leukemia [NCIt concept]
- Acute Myeloid Leukemia, Not Otherwise Specified [NCIt concept]
- Acute myeloblastic leukemia [ICD-10 Sub-category]
- Acute myeloid leukaemia [ICD-10 Sub-category (who)]
- Acute myeloid leukaemia [MedDRA Preferred Term]
- Acute myeloid leukaemia NOS [MedDRA LLT]
- Acute myeloid leukemia [HPO term]
- Acute myeloid leukemia [ORDO Disease]
- Acute myeloid leukemia [MedDRA LLT]
- Acute myeloid leukemia [ICD-O code]
- Acute myeloid leukemia [ICD-9 code]
- Acute myeloid leukemia (disorder) [SNOMED CT concept]
- Acute myeloid leukemia NOS [MedDRA LLT]
- Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Leukaemias acute myeloid [MedDRA High Level Term]
- Myeloid leukaemia, acute [MedDRA LLT]
- Myeloid leukemia, acute [MedDRA LLT]
- Myeloid leukemia, acute [ICD-9 code]
- acute myeloid leukemia [DO Concept]
- acute myeloid leukemia [Disease (Nov.)]
- acute myeloid leukemia [MedlinePlus Topic]
- acute myeloid leukemia [SNOMED Notion]
- leukemia, myeloid, acute [MeSH Descriptor]
- leukemia, myeloid, acute [MeSH concept]
DO Cross reference
- acute myeloid leukemia [DO Concept]
Genes related to phenotype
- Ccaat/enhancer-binding protein, alpha [OMIM gene]
- Cysteine-rich hydrophobic domain protein 2 [OMIM gene]
- Dna methyltransferase 3a [OMIM gene]
- Ets variant transcription factor 6 [OMIM gene]
- Fms-related tyrosine kinase 3 [OMIM gene]
- Gata-binding protein 2 [OMIM gene]
- Janus kinase 2 [OMIM gene]
- Kit protooncogene, receptor tyrosine kinase [OMIM gene]
- Kras protooncogene, gtpase [OMIM gene]
- Lim domain-containing preferred translocation partner in lipoma [OMIM gene]
- Mllt10 histone lysine methyltransferase dot1l cofactor [OMIM gene]
- Nucleophosmin/nucleoplasmin family, member 1 [OMIM gene]
- Nucleoporin, 214-kd [OMIM gene]
- Phosphatidylinositol-binding clathrin assembly protein [OMIM gene]
- Runt-related transcription factor 1 [OMIM gene]
- Telomerase reverse transcriptase [OMIM gene]
HPO term(s)
- Acute myeloid leukemia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Familial acute myelogenous leukemia [HPO term]
- Somatic mutation [HPO term]
ORDO concept(s)
- Acute leukemia of ambiguous lineage [ORDO Disease]
- Acute myeloid leukaemia with myelodysplasia-related features [ORDO Disease]
- Acute myeloid leukemia [ORDO Disease]
- Acute myeloid leukemia with CEBPA somatic mutations [ORDO Disease]
- Acute myeloid leukemia with recurrent genetic anomaly [ORDO Disease]
- Acute undifferentiated leukemia [ORDO Disease]
- Inherited acute myeloid leukemia [ORDO Disease]
- Mixed phenotype acute leukemia [ORDO Disease]
- Therapy related acute myeloid leukemia and myelodysplastic syndrome [ORDO Disease]
- Unclassified acute myeloid leukemia [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Acute Myeloid Leukemia [NCIt concept]
- Acute Myeloid Leukemia, Not Otherwise Specified [NCIt concept]
- Acute granulocytic leukaemia [MedDRA LLT]
- Acute granulocytic leukemia [MedDRA LLT]
- Acute megakaryocytic leukemia [HPO term]
- Acute myeloblastic leukaemia [MedDRA LLT]
- Acute myeloblastic leukemia [MedDRA LLT]
- Acute myeloblastic leukemia [ICD-10 Sub-category]
- Acute myelocytic leukaemia [MedDRA LLT]
- Acute myelocytic leukemia [MedDRA LLT]
- Acute myeloid leukaemia [ICD-10 Sub-category (who)]
- Acute myeloid leukaemia [MedDRA Preferred Term]
- Acute myeloid leukaemia NOS [MedDRA LLT]
- Acute myeloid leukemia [MedDRA LLT]
- Acute myeloid leukemia [ORDO Disease]
- Acute myeloid leukemia [ICD-O code]
- Acute myeloid leukemia [HPO term]
- Acute myeloid leukemia [LOINC component]
- Acute myeloid leukemia (disorder) [SNOMED CT concept]
- Acute myeloid leukemia (morphologic abnormality) [SNOMED CT concept]
- Acute myeloid leukemia - category (morphologic abnormality) [SNOMED CT concept]
- Acute myeloid leukemia NOS [MedDRA LLT]
- Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Leukaemia myeloblastic acute [MedDRA LLT]
- Leukaemias acute myeloid [MedDRA High Level Term]
- Leukemia myeloblastic acute [MedDRA LLT]
- Myeloid leukaemia, acute [MedDRA LLT]
- Myeloid leukemia, acute [MedDRA LLT]
- Myeloid leukemia, acute [ICD-9 code]
- Non-lymphoblastic leukaemia acute [MedDRA LLT]
- Non-lymphoblastic leukemia acute [MedDRA LLT]
- acute myeloid leukemia [SNOMED Notion]
- acute myeloid leukemia [DO Concept]
- acute myeloid leukemia [Disease (Nov.)]
- acute myeloid leukemia [MedlinePlus Topic]
- leukemia, myeloid, acute [MeSH Descriptor]
- leukemia, myeloid, acute [MeSH concept]

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