ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Neurofibromatosis type 3

Acute myeloid leukemia with t(8;16)(p11;p13) translocation


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCB1	(0.83)	CREBBP

Citations in the biomedical literature:

Neurofibromatosis type 3		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - 1 MeSH reference: C536641		External references: No OMIM references No MeSH references

No signs/symptoms info available.