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Acute biphenotypic leukemia
2 associated genes
24 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor B-cell acute lymphoblastic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myeloid leukemia with 11q23 abnormalities
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
Acute undifferentiated leukemia
Bilineal acute leukemia
Minimally differentiated acute myeloblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Wiedemann-Steiner syndrome
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
1 MeSH reference: D015456
Gene symbol UniProt reference OMIM reference
FLT3 P36888136351
KMT2A Q03164159555
No signs/symptoms info available.