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Intravascular large B-cell lymphoma
2 associated genes
98 connected diseases
No signs/symptoms info
Disease Type of connection
Follicular lymphoma
Primary mediastinal large B-cell lymphoma
Noonan syndrome
Familial pancreatic carcinoma
Familial isolated dilated cardiomyopathy
Pilocytic astrocytoma
Amyotrophic lateral sclerosis
Acute promyelocytic leukemia
MODY syndrome
LEOPARD syndrome
Essential thrombocythemia
Familial prostate cancer
Zonular cataract
Distal 22q11.2 microdeletion syndrome
Costello syndrome
Juvenile myelomonocytic leukemia
Linear nevus sebaceus syndrome
Coffin-Siris syndrome
Pseudohypoaldosteronism type 2E
Microphthalmia, Lenz type
Oculofaciocardiodental syndrome
2q37 microdeletion syndrome
Adrenocortical carcinoma
Autoimmune lymphoproliferative syndrome with recurrent infections
B-cell chronic lymphocytic leukemia
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Peters anomaly
Precursor B-cell acute lymphoblastic leukemia
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Behavioral variant of frontotemporal dementia
Early-onset autosomal dominant Alzheimer disease
Muscular dystrophy, Selcen type
Progressive non-fluent aphasia
Semantic dementia
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
Vitiligo-associated autoimmune disease
Burkitt lymphoma
Cardiofaciocutaneous syndrome
Hereditary nonpolyposis colon cancer
Precursor T-cell acute lymphoblastic leukemia
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Familial dementia, British type
Familial dementia, Danish type
Pseudohypoaldosteronism type 2B
Spinocerebellar ataxia type 15 / 16
Spinocerebellar ataxia type 29
Alternating hemiplegia of childhood
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
Short rib-polydactyly syndrome, Verma-Naumoff type
Spinocerebellar ataxia type 6
Wolcott-Rallison syndrome
Xeroderma pigmentosum complementation group G
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Young adult-onset Parkinsonism
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Carnitine palmitoyl transferase 1A deficiency
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Familial rhabdoid tumor
Fatal infantile hypertonic myofibrillar myopathy
Fleck corneal dystrophy
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Posterior polar cataract
Wolfram syndrome
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Autosomal thrombocytopenia with normal platelets
Myelofibrosis with myeloid metaplasia
Acrokeratosis verruciformis of Hopf
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Autoimmune lymphoproliferative syndrome
Darier disease
Large congenital melanocytic nevus
Phakomatosis pigmentokeratotica
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
- Angioendotheliomatosis proliferans systemisata
- Angiotropic large cell lymphoma
- Intravascular lymphomatosis
- Malignant angioendotheliomatosis
- Tappeiner-Pfleger disease

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
BCL2 P10415151430
BCL6 P41182109565
No signs/symptoms info available.