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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Kleefstra syndrome due to a point mutation
Primary mediastinal large B-cell lymphoma

EHMT1 BCL6


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EHMT1
(0.72)
BCL6



Citations in the biomedical literature:


Kleefstra syndrome due to a point mutation
EHMT1
Primary mediastinal large B-cell lymphoma
BCL6



Kleefstra syndrome due to a point mutation
Primary mediastinal large B-cell lymphoma

Synonym(s):
(no synonyms)

Synonym(s):
- Large cell lymphoma of the mediastinum
- Med-DLBCL
- Mediastinal diffuse large-cell lymphoma with sclerosis
- Primary mediastinal clear cell lymphoma of B-cell type

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic 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:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.