ODCs

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

PROTEIN INTERACTIONS: 1

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

Burkitt lymphoma

Connective tissue disorder due to lysyl hydroxylase-3 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYC	(0.72)	PLOD3

Citations in the biomedical literature:

Burkitt lymphoma		Connective tissue disorder due to lysyl hydroxylase-3 deficiency
	Synonym(s): - Small non-cleaved cell lymphoma		Synonym(s): - Bone fragility-contractures-arterial rupture-deafness syndrome - Connective tissue disorder due to LH3 deficiency

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.