Mantle cell lymphoma |
Familial platelet syndrome with predisposition to acute myelogenous leukemia |
ATM | RUNX1 | |||
CCND1 | ||||
IGH | (UniProt) |
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
CCND1 | (0.52) | RUNX1 | |
Citations in the biomedical literature:
Mantle cell lymphoma |
Familial platelet syndrome with predisposition to acute myelogenous leukemia |
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Synonym(s): - LCM- MCL - Mantle zone lymphoma | Synonym(s): - FPD/AML syndrome- FPS/AML syndrome - Familial platelet disorder with associated myeloid malignancy - Familial platelet syndrome | ||
Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease | Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare oncologic disease | ||
Classification (ICD10): - Neoplasms -
| Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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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: no data available 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 | |
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 platelet syndrome with predisposition to acute myelogenous leukemia | |
(no data available) |