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Minimally differentiated acute myeloblastic leukemia
1 associated gene
20 connected diseases
No signs/symptoms info
Disease Type of connection
Acute biphenotypic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute myelomonocytic leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Juvenile myelomonocytic leukemia
Autosomal agammaglobulinemia
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
SHORT syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Cherubism
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
FLT3 P36888136351
No signs/symptoms info available.