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Acute myeloid leukemia with t(8;21)(q22;q22) translocation
5 associated genes
193 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor B-cell acute lymphoblastic leukemia
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloblastic leukemia with maturation
Precursor T-cell acute lymphoblastic leukemia
Chronic myeloid leukemia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Isolated delta-storage pool disease
Acute myeloid leukemia with CEBPA somatic mutations
Inherited acute myeloid leukemia
Gastrointestinal stromal tumor
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
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Minimally differentiated acute myeloblastic leukemia
Nodular urticaria pigmentosa
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
Autosomal agammaglobulinemia
Acute promyelocytic leukemia
Juvenile myelomonocytic leukemia
Noonan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Hypocalcemic vitamin D-resistant rickets
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Extraskeletal myxoid chondrosarcoma
Coffin-Siris syndrome
Familial rhabdoid tumor
LEOPARD syndrome
SHORT syndrome
Distal 22q11.2 microdeletion syndrome
Acute megakaryoblastic leukemia without Down syndrome
Aneurysm - osteoarthritis syndrome
Berardinelli-Seip congenital lipodystrophy
Burkitt lymphoma
Cerebellar ataxia-deafness-narcolepsy syndrome
Cornelia de Lange syndrome
Papillary or follicular thyroid carcinoma
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Isolated brachycephaly
Isolated plagiocephaly
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Autosomal dominant nonsyndromic intellectual deficit
Inflammatory myofibroblastic tumor
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Translocation renal cell carcinoma
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Complete androgen insensitivity syndrome
Familial hypospadias
Familial isolated dilated cardiomyopathy
Kennedy disease
Partial androgen insensitivity syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
MODY syndrome
Congenital pulmonary alveolar proteinosis
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
Autosomal dominant severe congenital neutropenia
Dedifferentiated liposarcoma
Familial melanoma
Severe combined immunodeficiency due to LCK deficiency
Well-differentiated liposarcoma
Glucocorticoid resistance
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Uveal coloboma - cleft lip and palate - intellectual deficit
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Wilson-Turner syndrome
Dentatorubral pallidoluysian atrophy
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Recurrent infection due to specific granule deficiency
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Congenital communicating hydrocephalus
Craniosynostosis, Boston type
Multiple endocrine neoplasia type 1
Parietal foramina
Parietal foramina with cleidocranial dysplasia
Estrogen resistance syndrome
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Matthew-Wood syndrome
Myhre syndrome
Autosomal recessive primary microcephaly
Common variable immunodeficiency
Desmoid tumor
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Hepatocellular carcinoma, childhood-onset
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Autosomal dominant hypohidrotic ectodermal dysplasia
Combined immunodeficiency due to ZAP70 deficiency
PLCG2-associated antibody deficiency and immune dysregulation
X-linked lymphoproliferative disease
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Angelman syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Cerebellar ataxia - hypogonadism
Hereditary pheochromocytoma-paraganglioma
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Intellectual deficit - sparse hair - brachydactyly
Primary familial polycythemia
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Follicular lymphoma
Intravascular large B-cell lymphoma
Primary mediastinal large B-cell lymphoma
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Laron syndrome with immunodeficiency
Omenn syndrome
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Acute necrotizing encephalopathy of childhood
Adams-Oliver syndrome
Alexander disease type I
Alexander disease type II
Anophthalmia / microphthalmia - esophageal atresia
Atypical teratoid tumor
Autosomal dominant macrothrombocytopenia
Blepharophimosis-intellectual deficit syndrome, SBBYS type
Bohring-Opitz syndrome
Cataract-microcornea syndrome
Cerulean cataract
Colobomatous microphthalmia
Cone rod dystrophy
Desmoplastic small round cell tumor
Ewing sarcoma
Extraskeletal Ewing sarcoma
Familial acute necrotizing encephalopathy
Familial multiple meningioma
Genitopatellar syndrome
Hepatic veno-occlusive disease - immunodeficiency
Idiopathic hypereosinophilic syndrome
Isolated anophthalmia - microphthalmia
Leber congenital amaurosis
Meckel syndrome
Melanoma of soft part
Mowat-Wilson syndrome due to a point mutation
Mowat-Wilson syndrome due to monosomy 2q22
Myeloid neoplasm associated with PDGFRA rearrangement
Neurofibromatosis type 3
Peters anomaly
Pulverulent cataract
Romano-Ward syndrome
Septo-optic dysplasia
Young adult-onset Parkinsonism
Legius syndrome
Barth syndrome
Left ventricular noncompaction
Acute myeloid leukemia
B-cell chronic lymphocytic leukemia
Deafness - lymphedema - leukemia
Hyperinsulinism due to HNF1A deficiency
Kallmann syndrome
Mantle cell lymphoma
Monocytopenia with susceptibility to infections
Multiple myeloma
Myelodysplastic syndromes
Neurologic Waardenburg-Shah syndrome
T-B+ severe combined immunodeficiency due to JAK3 deficiency
Waardenburg syndrome type 2
Waardenburg-Shah syndrome
X-linked agammaglobulinemia
(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

No signs/symptoms info available.