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Mantle cell lymphoma

3 associated genes
7 signs/symptoms

PROTEIN INTERACTIONS: 1

Hereditary vascular retinopathy

1 OMIM reference -
1 associated gene
3 signs/symptoms

Mantle cell lymphoma

Hereditary vascular retinopathy

ATM	(UniProt - OMIM)		TREX1	(UniProt - OMIM)
CCND1	(UniProt - OMIM)
IGH	(UniProt)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ATM	(0.52)	TREX1

Citations in the biomedical literature:

Mantle cell lymphoma		Hereditary vascular retinopathy
	Synonym(s): - LCM - MCL - Mantle zone lymphoma		Synonym(s): - HVR - Hereditary vascular retinopathy - Raynaud phenomenon - migraine

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 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: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D020522		External references: 1 OMIM reference - No MeSH references

Mantle cell lymphoma		Hereditary vascular retinopathy
	Very frequent - Hematologic / blood / lymphatic cancer - Lymphadenopathy / polyadenopathies Frequent - Anorexia - Asthenia / fatigue / weakness - Bone marrow / medullar infiltration - Splenomegaly - Weight loss / loss of appetite / break in weight curve / general health alteration		Very frequent - Anomalies of eyes and vision - Autosomal dominant inheritance - Visual loss / blindness / amblyopia