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Wiedemann-Steiner syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Acute undifferentiated leukemia
1 associated gene
No signs/symptoms info
Wiedemann-Steiner syndrome
Acute undifferentiated leukemia

KMT2A
(UniProt - OMIM)
 KMT2A
(UniProt - OMIM)

COMMON
GENES 		KMT2A


Citations in the biomedical literature:


Wiedemann-Steiner syndrome
KMT2A
Acute undifferentiated leukemia



Wiedemann-Steiner syndrome
Acute undifferentiated leukemia

Synonym(s):
- Hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.