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Acute myeloid leukemia
1 OMIM reference -
1 associated gene
25 connected diseases
No signs/symptoms info
Disease Type of connection
Deafness - lymphedema - leukemia
Monocytopenia with susceptibility to infections
Myelodysplastic syndromes
Acute promyelocytic leukemia
Combined pituitary hormone deficiencies, genetic forms
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Autosomal agammaglobulinemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Primary biliary cirrhosis
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Autosomal dominant hyper-IgE syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cowden syndrome
Distal 22q11.2 microdeletion syndrome
Inherited acute myeloid leukemia
Proteus syndrome
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Synonym(s):
- AML
- Acute myelogenous leukemia
- Acute non-lymphoblastic leukemia
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D015470
Gene symbol UniProt reference OMIM reference
GATA2 P23769137295
No signs/symptoms info available.