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Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
4 associated genes
117 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute myeloblastic leukemia with maturation
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Gastrointestinal stromal tumor
Familial thoracic aortic aneurysm and aortic dissection
Acute biphenotypic leukemia
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Familial aortic dissection
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Minimally differentiated acute myeloblastic leukemia
Nodular urticaria pigmentosa
Piebaldism
Plaque-form urticaria pigmentosa
Pseudoxanthomatous diffuse cutaneous mastocytosis
Smouldering systemic mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Juvenile myelomonocytic leukemia
Chronic myeloid leukemia
Autosomal agammaglobulinemia
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
SHORT syndrome
Distal 22q11.2 microdeletion syndrome
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Cherubism
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Congenital pulmonary alveolar proteinosis
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Isolated delta-storage pool disease
Familial progressive hyper- and hypopigmentation
Familial progressive hyperpigmentation
Testicular non seminomatous germ cell tumor
Testicular seminomatous germ cell tumor
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Severe combined immunodeficiency due to LCK deficiency
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Congenital communicating hydrocephalus
Common variable immunodeficiency
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Inflammatory myofibroblastic tumor
Translocation renal cell carcinoma
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Burkitt lymphoma
Combined immunodeficiency due to ZAP70 deficiency
MODY syndrome
PLCG2-associated antibody deficiency and immune dysregulation
X-linked lymphoproliferative disease
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Primary familial polycythemia
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Acute promyelocytic leukemia
Laron syndrome with immunodeficiency
Omenn syndrome
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
APC-related attenuated familial adenomatous polyposis
Congenital glaucoma
Desmoid tumor
Familial adenomatous polyposis due to 5q22.2 microdeletion
Fanconi anemia
Gardner syndrome
Idiopathic hypereosinophilic syndrome
Juvenile glaucoma
Myeloid neoplasm associated with PDGFRA rearrangement
Turcot syndrome with polyposis
Cleidocranial dysplasia
Legius syndrome
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty
Moyamoya disease
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
T-B+ severe combined immunodeficiency due to JAK3 deficiency
X-linked agammaglobulinemia
Acral dystrophic epidermolysis bullosa
Autosomal recessive epidermolysis bullosa simplex
Baraitser-Winter syndrome
Centripetalis recessive dystrophic epidermolysis bullosa
Developmental malformations - deafness - dystonia
Dystrophic epidermolysis bullosa pruriginosa
Dystrophic epidermolysis bullosa, nails only
Early-onset autosomal dominant Alzheimer disease
Epidermolysis bullosa simplex superficialis
Generalized dominant dystrophic epidermolysis bullosa
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Hereditary sensory and autonomic neuropathy type 6
Pretibial dystrophic epidermolysis bullosa
Recessive dystrophic epidermolysis bullosa inversa
Recessive dystrophic epidermolysis bullosa-generalized other
Severe generalized recessive dystrophic epidermolysis bullosa
Transient bullous dermolysis of the newborn
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
CBFB Q13951121360
FLT3 P36888136351
KIT P10721164920
MYH11 P35749160745
No signs/symptoms info available.