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Acute megakaryoblastic leukemia without Down syndrome
2 associated genes
27 connected diseases
No signs/symptoms info
Disease Type of connection
Juvenile autosomal recessive medullary cystic kidney disease
Bardet-Biedl syndrome
Precursor B-cell acute lymphoblastic leukemia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Precursor T-cell acute lymphoblastic leukemia
Autosomal agammaglobulinemia
Autosomal dominant nonsyndromic intellectual deficit
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Chronic myeloid leukemia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Isolated delta-storage pool disease
Cornelia de Lange syndrome
Papillary or follicular thyroid carcinoma
Wilson-Turner syndrome
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Autosomal recessive limb-girdle muscular dystrophy type 2H
Acute promyelocytic leukemia
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Chudley-McCullough syndrome
Commissural facial cleft
Dentatorubral pallidoluysian atrophy
Hereditary sensory and autonomic neuropathy type 2
Pseudohypoaldosteronism type 2C
Tessier number 4 facial cleft

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
CBFA2T3 O75081603870
GLIS2 Q9BZE0608539
No signs/symptoms info available.