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 myelomonocytic leukemia

Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

FLT3	(UniProt - OMIM)		TUBB3	(UniProt - OMIM)
NPM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NPM1	(0.63)	TUBB3

Citations in the biomedical literature:

Acute myelomonocytic leukemia		Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation

	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: 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 1 MeSH reference: D015479		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.