ODCs

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

COMMON GENES: 1

2 associated genes
No signs/symptoms info

Wiedemann-Steiner syndrome

Acute biphenotypic leukemia

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

Citations in the biomedical literature:

Wiedemann-Steiner syndrome		Acute biphenotypic 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 1 MeSH reference: D015456

No signs/symptoms info available.