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Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
4 associated genes
No signs/symptoms info
COMMON GENES: 1
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
1 associated gene
4 signs/symptoms
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

CBFB
(UniProt - OMIM)
 KIT
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
KIT
(UniProt - OMIM)
MYH11
(UniProt - OMIM)

COMMON
GENES 		KIT


Citations in the biomedical literature:


Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
CBFB FLT3 KIT MYH11
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease



Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic 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: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Very frequent
- Acute leukemia
- Eosinophils anomalies / hypereosinophilia
- Mastocytosis
- Myeloproliferative syndrome / chronic leukemia



Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)

(no data available)