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Mantle cell lymphoma
3 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
Familial retinoblastoma
1 associated gene
No signs/symptoms info
Mantle cell lymphoma
Familial retinoblastoma

ATM
(UniProt - OMIM)
 RB1
(UniProt - OMIM)
CCND1
(UniProt - OMIM)
IGH
(UniProt)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CCND1
(0.9)
RB1


Citations in the biomedical literature:


Mantle cell lymphoma
ATM CCND1 IGH
Familial retinoblastoma
RB1



Mantle cell lymphoma
Familial retinoblastoma

Synonym(s):
- LCM
- MCL
- Mantle zone lymphoma
Synonym(s):
- Bilateral retinoblastoma
- Hereditary retinoblastoma
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -
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: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D020522
External references:
No OMIM references
No MeSH references
Mantle cell lymphoma

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



Familial retinoblastoma

(no data available)