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Extraskeletal Ewing sarcoma
4 associated genes
200 connected diseases
No signs/symptoms info
Disease Type of connection
Ewing sarcoma
Peripheral primitive neuroectodermal tumor
Melanoma of soft part
Extraskeletal myxoid chondrosarcoma
Isolated delta-storage pool disease
Paris-Trousseau thrombocytopenia
Desmoplastic small round cell tumor
Amyotrophic lateral sclerosis
Translocation renal cell carcinoma
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Cornelia de Lange syndrome
Precursor T-cell acute lymphoblastic leukemia
Familial pancreatic carcinoma
Hereditary breast and ovarian cancer syndrome
Retinitis pigmentosa
17q11 microdeletion syndrome
Precursor B-cell acute lymphoblastic leukemia
Severe combined immunodeficiency due to DNA-PKcs deficiency
Acute promyelocytic leukemia
Papillary or follicular thyroid carcinoma
Synovial sarcoma
Wolf-Hirschhorn syndrome
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Left ventricular noncompaction
Weaver syndrome
Williams syndrome
Acute basophilic leukemia
Beta-thalassemia - X-linked thrombocytopenia
Congenital erythropoietic porphyria
Thrombocytopenia with congenital dyserythropoietic anemia
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Ear-patella-short stature syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
ICF syndrome
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Burkitt lymphoma
Chronic myelomonocytic leukemia
Congenital dyserythropoietic anemia type IV
Congenital mesoblastic nephroma
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Autosomal dominant nonsyndromic intellectual deficit
Baraitser-Winter syndrome
Desmoid tumor
Developmental malformations - deafness - dystonia
Frontotemporal dementia with motor neuron disease
Hepatocellular carcinoma, childhood-onset
Juvenile amyotrophic lateral sclerosis
Myxoid / round cell liposarcoma
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Catecholaminergic polymorphic ventricular tachycardia
Complete androgen insensitivity syndrome
Familial hypospadias
Familial prostate cancer
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Kennedy disease
Partial androgen insensitivity syndrome
Primary peritoneal carcinoma
Charcot-Marie-Tooth disease type 4D
Cholesterol-ester transfer protein deficiency
Disseminated superficial actinic porokeratosis
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Heritable pulmonary arterial hypertension
Hyperimmunoglobulinemia D with periodic fever
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
Mevalonic aciduria
Myhre syndrome
Pulmonary capillary hemangiomatosis
Pulmonary venoocclusive disease
Pyruvate dehydrogenase E3-binding protein deficiency
Renal tubular dysgenesis of genetic origin
Cataract-microcornea syndrome
Cerulean cataract
Pulverulent cataract
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Aicardi-Goutières syndrome
Autosomal dominant spastic paraplegia type 13
Distal myopathy with vocal cord weakness
Dyschromatosis symmetrica hereditaria
Dyskeratosis congenita
Familial infantile bilateral striatal necrosis
Hoyeraal-Hreidarsson syndrome
Inflammatory myofibroblastic tumor
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Syndromic multisystem autoimmune disease due to Itch deficiency
X-linked epilepsy - learning disabilities - behavior disorders
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Estrogen resistance syndrome
X-linked dystonia-parkinsonism
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adrenocortical carcinoma
Adult-onset distal myopathy due to VCP mutation
Alternating hemiplegia of childhood
Aneurysm - osteoarthritis syndrome
Anophthalmia / microphthalmia - esophageal atresia
Autosomal dominant secondary polycythemia
B-cell chronic lymphocytic leukemia
Behavioral variant of frontotemporal dementia
Brugada syndrome
COFS syndrome
Cabezas syndrome
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss
Cerebellar ataxia-deafness-narcolepsy syndrome
Colobomatous microphthalmia
Common variable immunodeficiency
Dedifferentiated liposarcoma
Dentatorubral pallidoluysian atrophy
Essential thrombocythemia
Familial isolated dilated cardiomyopathy
Familial melanoma
Familial thoracic aortic aneurysm and aortic dissection
Fibronectin glomerulopathy
Giant cell glioblastoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Herpetic encephalitis
Inherited acute myeloid leukemia
Isolated ATP synthase deficiency
Isolated adermatoglyphia
Isolated anophthalmia - microphthalmia
Li-Fraumeni syndrome
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Multiple paragangliomas associated with polycythemia
Nager syndrome
Papilloma of choroid plexus
Progressive non-fluent aphasia
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Pseudohypoaldosteronism type 2E
Rapid-onset dystonia-parkinsonism
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Semantic dementia
Septo-optic dysplasia
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 19 / 22
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Well-differentiated liposarcoma
Xeroderma pigmentosum complementation group G
Young adult-onset Parkinsonism
Autosomal recessive limb-girdle muscular dystrophy type 2Q
Early-onset autosomal dominant Alzheimer disease
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex with pyloric atresia
Epidermolysis bullosa simplex, Ogna type
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
3-phosphoglycerate dehydrogenase deficiency
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Autosomal recessive malignant osteopetrosis
Autosomal recessive optic atrophy, OPA7 type
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Constitutional mismatch repair deficiency syndrome
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hereditary nonpolyposis colon cancer
Hutchinson-Gilford progeria syndrome
Kostmann syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Progeria-associated arthropathy
Richieri Costa-Pereira syndrome
- Extraosseous Ewing sarcoma
- Extraosseous Ewing tumor
- Extraskeletal Ewing tumor

Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
ERG P11308165080
EWSR1 Q01844133450
FLI1 Q01543193067
SMARCA5 O60264603375
No signs/symptoms info available.