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3 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
1 sign/symptom
Mantle cell lymphoma
Familial hypospadias

ATM AR
CCND1 MAMLD1
IGH


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CCND1
(0.9)
AR



Citations in the biomedical literature:


Mantle cell lymphoma
ATM CCND1 IGH
Familial hypospadias
AR MAMLD1



Mantle cell lymphoma
Familial hypospadias

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
1 MeSH reference: D020522
External references:
4 OMIM references -
No MeSH references

Mantle cell lymphoma
Familial hypospadias

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



Very frequent
- Hypospadias / epispadias / bent penis