ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Burkitt lymphoma

Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYC	(0.63)	PRG4

Citations in the biomedical literature:

Burkitt lymphoma		Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
	Synonym(s): - Small non-cleaved cell lymphoma		Synonym(s): - Arthropathy-camptodactyly syndrome - CACP syndrome - Jacobs syndrome - Pericarditis - arthropathy - camptodactyly

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): (no data available)

	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: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
	Very frequent - Autosomal recessive inheritance - Camptodactyly of fingers - Osteoarthritis - Pericardium anomalies / pericarditis / absence / cysts / pericardial effusion Occasional - Hepatomegaly / liver enlargement (excluding storage disease) - Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
Burkitt lymphoma
(no data available)