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3 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Mantle cell lymphoma
Familial rhabdoid tumor

ATM SMARCA4
CCND1 SMARCB1
IGH


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATM
(0.72)
SMARCB1



Citations in the biomedical literature:


Mantle cell lymphoma
ATM CCND1 IGH
Familial rhabdoid tumor
SMARCA4 SMARCB1



Mantle cell lymphoma
Familial rhabdoid tumor

Synonym(s):
- LCM
- MCL
- Mantle zone lymphoma

Synonym(s):
- RTPS
- Rhabdoid tumor predisposition syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic 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: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
1 MeSH reference: D020522
External references:
2 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 rhabdoid tumor

(no data available)