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Ewing sarcoma
1 OMIM reference -
5 associated genes
158 connected diseases
No signs/symptoms info
Disease Type of connection
Extraskeletal Ewing sarcoma
Peripheral primitive neuroectodermal tumor
Extraskeletal myxoid chondrosarcoma
Isolated delta-storage pool disease
Paris-Trousseau thrombocytopenia
Desmoplastic small round cell tumor
Melanoma of soft part
Translocation renal cell carcinoma
Amyotrophic lateral sclerosis
Familial pancreatic carcinoma
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Hereditary breast and ovarian cancer syndrome
Severe combined immunodeficiency due to DNA-PKcs deficiency
Retinitis pigmentosa
Precursor B-cell acute lymphoblastic leukemia
Acute promyelocytic leukemia
Precursor T-cell acute lymphoblastic leukemia
Early-onset autosomal dominant Alzheimer disease
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
Weaver 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
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
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
17q11 microdeletion syndrome
Chronic myelomonocytic leukemia
Congenital dyserythropoietic anemia type IV
Congenital mesoblastic nephroma
Fibrosarcoma
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
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
MULIBREY nanism
Mevalonic aciduria
Myhre syndrome
Pulmonary capillary hemangiomatosis
Pulmonary venoocclusive disease
Pyruvate dehydrogenase E3-binding protein deficiency
Renal tubular dysgenesis of genetic origin
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
Estrogen resistance syndrome
X-linked dystonia-parkinsonism
ADULT syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adrenocortical carcinoma
Alternating hemiplegia of childhood
Aneurysm - osteoarthritis syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Autosomal dominant secondary polycythemia
B-cell chronic lymphocytic leukemia
Bladder exstrophy
Brugada syndrome
COFS syndrome
Cabezas syndrome
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss
Common variable immunodeficiency
Cornelia de Lange syndrome
Dedifferentiated liposarcoma
Dentatorubral pallidoluysian atrophy
EEC syndrome
Essential thrombocythemia
Familial isolated dilated cardiomyopathy
Familial melanoma
Familial thoracic aortic aneurysm and aortic dissection
Fibronectin glomerulopathy
Giant cell glioblastoma
Gliosarcoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Herpetic encephalitis
Huntington disease
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Inherited acute myeloid leukemia
Isolated ATP synthase deficiency
Juvenile Huntington disease
Left ventricular noncompaction
Li-Fraumeni syndrome
Limb-mammary syndrome
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Multiple paragangliomas associated with polycythemia
Nager syndrome
Odontoleukodystrophy
Papillary or follicular thyroid carcinoma
Papilloma of choroid plexus
Peutz-Jeghers syndrome
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
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 19 / 22
Split hand-split foot malformation
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Well-differentiated liposarcoma
Wolf-Hirschhorn syndrome
Xeroderma pigmentosum complementation group G
Young adult-onset Parkinsonism
Autosomal recessive limb-girdle muscular dystrophy type 2Q
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex with pyloric atresia
Epidermolysis bullosa simplex, Ogna type
Autosomal recessive malignant osteopetrosis
Autosomal recessive optic atrophy, OPA7 type
Kostmann syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.