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CADDS
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intravascular large B-cell lymphoma
2 associated genes
No signs/symptoms info
CADDS
Intravascular large B-cell lymphoma

ABCD1
(UniProt - OMIM)
 BCL2
(UniProt - OMIM)
BCAP31
(UniProt - OMIM)
 BCL6
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BCAP31
(0.79)
BCL2


Citations in the biomedical literature:


CADDS
ABCD1 BCAP31
Intravascular large B-cell lymphoma
BCL2 BCL6



CADDS
Intravascular large B-cell lymphoma

Synonym(s):
- Contiguous ABCD1 DXS1357E deletion syndrome
- Zellweger-like contiguous gene deletion syndrome
Synonym(s):
- Angioendotheliomatosis proliferans systemisata
- Angiotropic large cell lymphoma
- Intravascular lymphomatosis
- Malignant angioendotheliomatosis
- Tappeiner-Pfleger disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare hepatic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.