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Burkitt lymphoma
1 OMIM reference -
1 associated gene
322 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor T-cell acute lymphoblastic leukemia
Precursor B-cell acute lymphoblastic leukemia
Hereditary nonpolyposis colon cancer
Retinitis pigmentosa
Isolated NADH-CoQ reductase deficiency
Familial isolated dilated cardiomyopathy
Constitutional mismatch repair deficiency syndrome
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Familial pancreatic carcinoma
Williams syndrome
Left ventricular noncompaction
Fanconi anemia
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Autosomal recessive primary microcephaly
Coffin-Siris syndrome
Familial rhabdoid tumor
Familial melanoma
Distal 22q11.2 microdeletion syndrome
Autosomal recessive centronuclear myopathy
Hereditary breast and ovarian cancer syndrome
LEOPARD syndrome
Noonan syndrome
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Autosomal dominant Emery-Dreifuss muscular dystrophy
Chronic myeloid leukemia
Leigh syndrome with leukodystrophy
Osteogenesis imperfecta type 3
Mosaic variegated aneuploidy syndrome
Amyotrophic lateral sclerosis
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
B-cell chronic lymphocytic leukemia
Baraitser-Winter syndrome
Bifunctional enzyme deficiency
Cornelia de Lange syndrome
Hereditary pheochromocytoma-paraganglioma
Familial prostate cancer
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Atypical teratoid tumor
Familial multiple meningioma
Mandibulofacial dysostosis-microcephaly syndrome
Neurofibromatosis type 3
Facial dysmorphism - immunodeficiency - livedo - short stature
Pilocytic astrocytoma
Acute promyelocytic leukemia
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Acute infantile liver failure-multisystemic involvement syndrome
Autosomal dominant optic atrophy plus syndrome
Autosomal dominant optic atrophy, classic type
Spinocerebellar ataxia type 17
Spinocerebellar ataxia type 36
Dedifferentiated liposarcoma
Intellectual deficit, X-linked, Turner type
Well-differentiated liposarcoma
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Anaplastic ependymoma
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Acrokeratosis verruciformis of Hopf
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Darier disease
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Distal hereditary motor neuropathy type 2
Extraskeletal Ewing sarcoma
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Fatal infantile lactic acidosis with methylmalonic aciduria
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Mitochondrial trifunctional protein deficiency
Progeria-associated arthropathy
Translocation renal cell carcinoma
Aneurysm - osteoarthritis syndrome
Ear-patella-short stature syndrome
Familial thoracic aortic aneurysm and aortic dissection
Branchio-oculo-facial syndrome
Lissencephaly due to TUBA1A mutation
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Blepharophimosis-intellectual deficit syndrome, MKB type
FG syndrome type 1
Follicular lymphoma
Intravascular large B-cell lymphoma
Melanoma of soft part
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
Acute myeloid leukemia with CEBPA somatic mutations
Inherited acute myeloid leukemia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
17p13.3 microduplication syndrome
ALDH18A1-related De Barsy syndrome
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute necrotizing encephalopathy of childhood
Acute neonatal citrullinemia type I
Adams-Oliver syndrome
Adrenocortical carcinoma
Adult-onset citrullinemia type I
Atrial septal defect, ostium secundum type
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal dominant nonsyndromic intellectual deficit
Autosomal dominant spastic paraplegia type 13
Blackfan-Diamond anemia
CLN1 disease
Catecholaminergic polymorphic ventricular tachycardia
Chronic intestinal pseudoobstruction
Citrullinemia type II
Congenital atransferrinemia
Congenital short bowel syndrome
Congenital valvular dysplasia
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
D,L-2-hydroxyglutaric aciduria
Distal 17p13.3 microdeletion syndrome
Distal monosomy 12p
Ehlers-Danlos syndrome with periventricular heterotopia
Epileptic encephalopathy with global cerebral demyelination
Essential thrombocythemia
Extraskeletal myxoid chondrosarcoma
Familial acute necrotizing encephalopathy
Familial dysautonomia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Familial vesicoureteral reflux
Fatal infantile cytochrome C oxidase deficiency
Fibronectin glomerulopathy
Frontometaphyseal dysplasia
Generalized congenital lipodystrophy with myopathy
Giant cell glioblastoma
Glutaryl-CoA dehydrogenase deficiency
Gyrate atrophy of choroid and retina
Hereditary sensory and autonomic neuropathy type 1
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Hypotonia with lactic acidemia and hyperammonemia
Inflammatory myofibroblastic tumor
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Isolated CoQ-cytochrome C reductase deficiency
Isolated brachycephaly
Isolated delta-storage pool disease
Isolated plagiocephaly
Leigh syndrome with cardiomyopathy
Li-Fraumeni syndrome
MALT lymphoma
Mandibular hypoplasia-deafness-progeroid syndrome
Miller-Dieker syndrome
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Neonatal intrahepatic cholestasis due to citrin deficiency
Noonan syndrome-like disorder with loose anagen hair
Osteodysplasty, Melnick-Needles type
Osteogenesis imperfecta type 2
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Papillary or follicular thyroid carcinoma
Papilloma of choroid plexus
Pediatric systemic lupus erythematosus
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Periventricular nodular heterotopia
Rare isolated myopia
Severe combined immunodeficiency due to DNA-PKcs deficiency
Terminal osseous dysplasia - pigmentary defects
Xanthinuria type I
Xeroderma pigmentosum complementation group B
Cerebellar ataxia - hypogonadism
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Multiple endocrine neoplasia type 1
Zollinger-Ellison syndrome
17q11 microdeletion syndrome
Familial retinoblastoma
Monosomy 13q14
Split hand-split foot malformation
Unilateral retinoblastoma
22q11.2 deletion syndrome
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Alpers syndrome
Amyotrophic lateral sclerosis type 4
Ataxia-telangiectasia variant
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant centronuclear myopathy
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant limb-girdle muscular dystrophy type 1F
Autosomal dominant progressive external ophthalmoplegia
Autosomal recessive ataxia, Beauce type
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive limb-girdle muscular dystrophy type 2J
Autosomal recessive myogenic arthrogryposis multiplex congenita
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal recessive progressive external ophthalmoplegia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Autosomal recessive spastic paraplegia type 56
Axenfeld anomaly
Axenfeld-Rieger syndrome
Behçet disease
Borjeson-Forssman-Lehmann syndrome
Bruck syndrome
CLN2 disease
Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
Cardiomyopathy - hypotonia - lactic acidosis
Charcot-Marie-Tooth disease type 4G
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
Chronic granulomatous disease
Chronic myelomonocytic leukemia
Chuvash erythrocytosis
Cleidocranial dysplasia
Combined cervical dystonia
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency
Combined immunodeficiency with skin granulomas
Combined oxidative phosphorylation defect type 4
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy
Congenital fibrosis of extraocular muscles
Congenital mesoblastic nephroma
Congenital myasthenic syndromes with glycosylation defect
Congenital stationary night blindness
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Craniofrontonasal dysplasia
Distal hereditary motor neuropathy type 7
Distal monosomy 15q
Distal myopathy with vocal cord weakness
Early-onset myopathy with fatal cardiomyopathy
Estrogen resistance syndrome
FASTKD2-related infantile mitochondrial encephalomyopathy
Familial atrial fibrillation
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Greenberg dysplasia
Griscelli disease type 1
Griscelli disease type 3
Hereditary hypercarotenemia and vitamin A deficiency
Hereditary proximal myopathy with early respiratory failure
Hypocalcemic vitamin D-resistant rickets
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Idiopathic pulmonary fibrosis
Immunodeficiency due to an early component of complement deficiency
Immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
Isolated adermatoglyphia
Isolated cytochrome C oxidase deficiency
Joubert syndrome
Juvenile myelomonocytic leukemia
Keratosis palmoplantaris striata
Lethal acantholytic epidermolysis bullosa
Leukocyte adhesion deficiency type III
Lymphedema - distichiasis
Mantle cell lymphoma
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty
Mitochondrial neurogastrointestinal encephalomyopathy
Mucopolysaccharidosis type 6, rapidly progressing
Mucopolysaccharidosis type 6, slowly progressing
Neuroectodermal melanolysosomal disease
Nijmegen breakage syndrome-like disorder
Non-spherocytic hemolytic anemia due to hexokinase deficiency
Occipital encephalocele
Omenn syndrome
Perrault syndrome
Perry syndrome
Peters anomaly
Primary Fanconi syndrome
Primary biliary cirrhosis
Primary ciliary dyskinesia
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Quebec platelet disorder
Recessive mitochondrial ataxia syndrome
Reynolds syndrome
Rieger anomaly
Ring dermoid of cornea
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Severe combined immunodeficiency due to complete RAG1 / 2 deficiency
Severe intellectual deficit and progressive spastic paraplegia
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Spinocerebellar ataxia with axonal neuropathy type 2
Spinocerebellar ataxia with epilepsy
Syndromic diarrhea
TARP syndrome
Tibial muscular dystrophy
Von Hippel-Lindau disease
Wiskott-Aldrich syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
X-linked distal arthrogryposis multiplex congenita
X-linked intellectual deficit - cerebellar hypoplasia
X-linked sideroblastic anemia - ataxia
Intellectual deficit - sparse hair - brachydactyly
Char syndrome
Developmental malformations - deafness - dystonia
Polymicrogyria with optic nerve hypoplasia
Weaver syndrome
Cardiofaciocutaneous syndrome
Young adult-onset Parkinsonism
- Small non-cleaved cell lymphoma

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: sporadic
External references:
1 OMIM reference -
2 MeSH references: D002051 / D008228

Gene symbol UniProt reference OMIM reference
MYC P01106190080
No signs/symptoms info available.