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Acute myeloid leukemia with multilineage dysplasia
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Acquired idiopathic sideroblastic anemia
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Refractory anemia
Refractory anemia with excess blasts
Autosomal agammaglobulinemia
Precursor B-cell acute lymphoblastic leukemia
Coffin-Siris syndrome
Familial rhabdoid tumor
Methylmalonic acidemia with homocystinuria, type cblX
X-linked non-syndromic intellectual deficit
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
TET2 Q6N021612839
No signs/symptoms info available.