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Acute myeloid leukemia with CEBPA somatic mutations
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary pheochromocytoma-paraganglioma
6 OMIM references -
7 associated genes
No signs/symptoms info
Acute myeloid leukemia with CEBPA somatic mutations
Hereditary pheochromocytoma-paraganglioma

CEBPA
(UniProt - OMIM)
 MAX
(UniProt - OMIM)
SDHA
(UniProt - OMIM)
SDHAF2
(UniProt - OMIM)
SDHB
(UniProt - OMIM)
SDHC
(UniProt - OMIM)
SDHD
(UniProt - OMIM)
TMEM127
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CEBPA
(0.68)
MAX


Citations in the biomedical literature:


Acute myeloid leukemia with CEBPA somatic mutations
CEBPA
Hereditary pheochromocytoma-paraganglioma
MAX SDHA SDHAF2 SDHB SDHC SDHD
TMEM127



Acute myeloid leukemia with CEBPA somatic mutations
Hereditary pheochromocytoma-paraganglioma

Synonym(s):
- AML with CEBPA somatic mutations
Synonym(s):
- Familial pheochromocytoma-paraganglioma
- SDHx-related paraganglioma-pheochromocytoma
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.