ODCs

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3 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Parietal foramina

Acute myeloid leukemia with CEBPA somatic mutations

ALX4	(UniProt - OMIM)		CEBPA	(UniProt - OMIM)
MSX2	(UniProt - OMIM)


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

Citations in the biomedical literature:

Parietal foramina		Acute myeloid leukemia with CEBPA somatic mutations
	Synonym(s): - Catlin marks - Enlarged parietal foramina - Foramina parietalia permagna - Hereditary cranium bifidum		Synonym(s): - AML with CEBPA somatic mutations

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.