Cytoscape Web
Click node...

Primary mediastinal large B-cell lymphoma
1 associated gene
41 connected diseases
No signs/symptoms info
Disease Type of connection
Follicular lymphoma
Intravascular large B-cell lymphoma
Acute promyelocytic leukemia
Coffin-Siris syndrome
Microphthalmia, Lenz type
Oculofaciocardiodental syndrome
2q37 microdeletion syndrome
Peters anomaly
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Pseudohypoaldosteronism type 2B
Alternating hemiplegia of childhood
Amyotrophic lateral sclerosis
Autosomal recessive nonsyndromic intellectual deficit
Benign paroxysmal torticollis of infancy
COFS syndrome
Cranioectodermal dysplasia
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Hereditary sensory and autonomic neuropathy type 1
Hyperinsulinism due to HNF1A deficiency
Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies
Kleefstra syndrome due to 9q34 microdeletion
Kleefstra syndrome due to a point mutation
MODY syndrome
Short rib-polydactyly syndrome, Verma-Naumoff type
Spinocerebellar ataxia type 6
Wolcott-Rallison syndrome
Xeroderma pigmentosum complementation group G
Zonular cataract
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Familial rhabdoid tumor
Fleck corneal dystrophy
Pseudohypoaldosteronism type 2E
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Distal 22q11.2 microdeletion syndrome
LEOPARD syndrome
Noonan syndrome
Pilocytic astrocytoma
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
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 hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
BCL6 P41182109565
No signs/symptoms info available.