ODCs

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1 OMIM reference -
4 associated genes
14 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Follicular lymphoma

Fatal infantile hypertonic myofibrillar myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	BCL2	(0.63)	CRYAB

Citations in the biomedical literature:

Follicular lymphoma		Fatal infantile hypertonic myofibrillar myopathy

	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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

	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
Fatal infantile hypertonic myofibrillar myopathy
(no data available)