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3 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Mantle cell lymphoma
Familial lipoprotein lipase deficiency

ATM LPL
CCND1
IGH


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CCND1
(0.63)
LPL



Citations in the biomedical literature:


Mantle cell lymphoma
ATM CCND1 IGH
Familial lipoprotein lipase deficiency
LPL



Mantle cell lymphoma
Familial lipoprotein lipase deficiency

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

Synonym(s):
- LPL deficiency

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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:
(no data available)

External references:
No OMIM references
1 MeSH reference: D020522
External references:
1 OMIM reference -
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 lipoprotein lipase deficiency

(no data available)