Cytoscape Web
Click node...

Myelodysplastic syndromes
1 OMIM reference -
2 associated genes
32 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloid leukemia
Deafness - lymphedema - leukemia
Monocytopenia with susceptibility to infections
Acute promyelocytic leukemia
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Aneurysm - osteoarthritis syndrome
Combined pituitary hormone deficiencies, genetic forms
Familial thoracic aortic aneurysm and aortic dissection
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
2q37 microdeletion syndrome
Anophthalmia / microphthalmia - esophageal atresia
Autosomal agammaglobulinemia
Colobomatous microphthalmia
Isolated anophthalmia - microphthalmia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Primary biliary cirrhosis
Septo-optic dysplasia
Autosomal dominant hyper-IgE syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cowden syndrome
Distal 22q11.2 microdeletion syndrome
Inherited acute myeloid leukemia
Proteus syndrome
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D009190
Gene symbol UniProt reference OMIM reference
GATA2 P23769137295
MECOM Q03112165215
No signs/symptoms info available.