ODCs

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5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Parietal foramina with cleidocranial dysplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CEBPA	(0.76)	MSX2

Citations in the biomedical literature:

Acute myeloid leukemia with t(8;21)(q22;q22) translocation		Parietal foramina with cleidocranial dysplasia
	Synonym(s): (no synonyms)		Synonym(s): - Parietal foramina with cleidocranial dysostosis

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic 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: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.