ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Familial paroxysmal ataxia

Intravascular large B-cell lymphoma

CACNA1A	(UniProt - OMIM)		BCL2	(UniProt - OMIM)
			BCL6	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.72)	BCL6

Citations in the biomedical literature:

Familial paroxysmal ataxia		Intravascular large B-cell lymphoma
	Synonym(s): - Episodic ataxia type 2		Synonym(s): - Angioendotheliomatosis proliferans systemisata - Angiotropic large cell lymphoma - Intravascular lymphomatosis - Malignant angioendotheliomatosis - Tappeiner-Pfleger disease

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

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

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

No signs/symptoms info available.