ODCs

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2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Acute biphenotypic leukemia

Wiedemann-Steiner syndrome

FLT3	(UniProt - OMIM)		KMT2A	(UniProt - OMIM)
KMT2A	(UniProt - OMIM)

Citations in the biomedical literature:

Acute biphenotypic 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 1 MeSH reference: D015456		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.