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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
Juvenile glaucoma
6 OMIM references -
2 associated genes
No signs/symptoms info
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Juvenile glaucoma

CBFB
(UniProt - OMIM)
 CYP1B1
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
 MYOC
(UniProt - OMIM)
KIT
(UniProt - OMIM)
MYH11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYH11
(0.63)
MYOC


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
Juvenile glaucoma
CYP1B1 MYOC



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

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: normal
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.