Cytoscape Web
Click node...

Wiedemann-Steiner syndrome
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Acute biphenotypic leukemia
Acute myeloid leukemia with 11q23 abnormalities
Acute undifferentiated leukemia
Bilineal acute leukemia
Precursor B-cell acute lymphoblastic leukemia
Synonym(s):
- Hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KMT2A Q03164159555
No signs/symptoms info available.