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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
PROTEIN INTERACTIONS: 1
Moyamoya disease
4 OMIM references -
2 associated genes
6 signs/symptoms
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Moyamoya disease

CBFB
(UniProt - OMIM)
 ACTA2
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
 RNF213
(UniProt - OMIM)
KIT
(UniProt - OMIM)
MYH11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYH11
(0.56)
ACTA2


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
Moyamoya disease
ACTA2 RNF213



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

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
2 MeSH references: C536991 / D009072
Moyamoya disease

Very frequent
- Autosomal recessive inheritance
- Vascular anomalies of skin / mucosae

Frequent
- Cerebral vascular anomalies
- Dilated cerebral ventricles without hydrocephaly
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Seizures / epilepsy / absences / spasms / status epilepticus



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

(no data available)