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Follicular lymphoma

1 OMIM reference -
4 associated genes
14 signs/symptoms

PROTEIN INTERACTIONS: 1

Familial paroxysmal ataxia

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

Follicular lymphoma

Familial paroxysmal ataxia

BCL2	(UniProt - OMIM)		CACNA1A	(UniProt - OMIM)
BCL6	(UniProt - OMIM)
HLA-DRB1	(UniProt - OMIM)
IGH	(UniProt)


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

Citations in the biomedical literature:

Follicular lymphoma		Familial paroxysmal ataxia
	Synonym(s): (no synonyms)		Synonym(s): - Episodic ataxia type 2

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

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

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: adulthood Average age of death: adult Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D008224		External references: 1 OMIM reference - No MeSH references

Follicular lymphoma
	Very frequent - Fever / chilling - Hematologic / blood / lymphatic cancer - Hyperhidrosis / increased sweating - Lymphadenopathy / polyadenopathies - Weight loss / loss of appetite / break in weight curve / general health alteration Frequent - Asthenia / fatigue / weakness - Mediastinal / hilar adenopathies - Splenomegaly Occasional - Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax - Anomalies of skin, subcutaneous tissue and mucosae - Bone marrow / medullar infiltration - Lymphedema - Meningitis / meningeal syndrome - Structural anomaly of the peritoneum
Familial paroxysmal ataxia
(no data available)