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

KMT2A KMT2A


COMMON
GENES
KMT2A



Citations in the biomedical literature:


Acute undifferentiated leukemia
KMT2A
Wiedemann-Steiner syndrome



Acute undifferentiated leukemia
Wiedemann-Steiner syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.