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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
7 signs/symptoms
Craniopharyngioma
Mantle cell lymphoma

BRAF ATM
CTNNB1 CCND1
IGH


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.62)
CCND1



Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Mantle cell lymphoma
ATM CCND1 IGH



Craniopharyngioma
Mantle cell lymphoma

Synonym(s):
(no synonyms)

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

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: multigenic/multifactorial

External references:
No OMIM references
1 MeSH reference: D003397
External references:
No OMIM references
1 MeSH reference: D020522

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



Craniopharyngioma

(no data available)