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Mantle cell lymphoma
3 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
LIG4 syndrome
1 OMIM reference -
1 associated gene
34 signs/symptoms
Mantle cell lymphoma
LIG4 syndrome

ATM
(UniProt - OMIM)
 LIG4
(UniProt - OMIM)
CCND1
(UniProt - OMIM)
IGH
(UniProt)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ATM
(0.63)
LIG4


Citations in the biomedical literature:


Mantle cell lymphoma
ATM CCND1 IGH
LIG4 syndrome
LIG4



Mantle cell lymphoma
LIG4 syndrome

Synonym(s):
- LCM
- MCL
- Mantle zone lymphoma
Synonym(s):
- DNA ligase IV deficiency
- Ligase 4 syndrome
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: neonatal/infancy
Average age of death: young adult
Type of inheritance: autosomal recessive
External references:
No OMIM references
1 MeSH reference: D020522
External references:
1 OMIM reference -
No MeSH references
COMMON
SIGNS 		- Lymphadenopathy / polyadenopathies

Mantle cell lymphoma
LIG4 syndrome

Very frequent
- Hematologic / blood / lymphatic cancer

Frequent
- Anorexia
- Asthenia / fatigue / weakness
- Bone marrow / medullar infiltration
- Splenomegaly
- Weight loss / loss of appetite / break in weight curve / general health alteration



Very frequent
- Autosomal recessive inheritance
- Chromosome breakage
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Immunodeficiency / increased susceptibility to infections / recurrent infections
- Microcephaly

Frequent
- Acute leukemia
- Anomalies of skin, subcutaneous tissue and mucosae
- Bone marrow failure / pancytopenia
- Brachycephaly / flat occiput
- Broad nasal root
- Epicanthic folds
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long / large / bulbous nose
- Low hair line-front
- Lymphoma
- Micrognathia / retrognathia / micrognathism / retrognathism
- Narrow forehead
- Skin photosensitivity
- Telecanthus / canthal dystopy
- Thin / retracted lips
- Upslanted palpebral fissures / mongoloid slanting palpebral fissures

Occasional
- Anomalies of bones / skeletal anomalies
- Clinodactyly of fifth finger
- Hepatomegaly / liver enlargement (excluding storage disease)
- Hyperleukocytosis / leukocytosis
- Hypothyroidy
- Insulin-independent / type 2 diabetes
- Malabsorption / chronic diarrhea / steatorrhea
- Micropenis / small penis / agenesis
- Severe combined immune deficiency syndrome / SCID
- Telangiectasiae of the skin
- Undescended / ectopic testes / cryptorchidia / unfixed testes