ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Acute biphenotypic leukemia

Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema

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


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLT3	(0.68)	IKBKG

Citations in the biomedical literature:

Acute biphenotypic leukemia		Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
	Synonym(s): (no synonyms)		Synonym(s): - OL-EDA-ID

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease - Rare skin disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: x-linked recessive

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

No signs/symptoms info available.