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Extraskeletal myxoid chondrosarcoma
1 OMIM reference -
5 associated genes
151 connected diseases
No signs/symptoms info
Disease Type of connection
Amyotrophic lateral sclerosis
Papillary or follicular thyroid carcinoma
Ewing sarcoma
Extraskeletal Ewing sarcoma
Desmoplastic small round cell tumor
Melanoma of soft part
Hereditary motor and sensory neuropathy, Okinawa type
Isolated brachycephaly
Isolated plagiocephaly
Spastic paraplegia-optic atrophy-neuropathy syndrome
Precursor B-cell acute lymphoblastic leukemia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cabezas syndrome
Pseudohypoaldosteronism type 2E
Precursor T-cell acute lymphoblastic leukemia
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Alobar holoprosencephaly
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
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
17q11 microdeletion syndrome
Weaver syndrome
Familial pancreatic carcinoma
Common variable immunodeficiency
Spinocerebellar ataxia type 17
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
X-linked dystonia-parkinsonism
Cornelia de Lange syndrome
Herpetic encephalitis
Isolated delta-storage pool disease
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
Hereditary breast and ovarian cancer syndrome
Schizencephaly
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Autosomal agammaglobulinemia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Catecholaminergic polymorphic ventricular tachycardia
Charcot-Marie-Tooth disease type 4D
Cholesterol-ester transfer protein deficiency
Disseminated superficial actinic porokeratosis
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
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
Burkitt lymphoma
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Syndromic multisystem autoimmune disease due to Itch deficiency
Estrogen resistance syndrome
Acute myeloid leukemia with CEBPA somatic mutations
Acute promyelocytic leukemia
Adrenocortical carcinoma
Alternating hemiplegia of childhood
Aneurysm - osteoarthritis syndrome
Anophthalmia / microphthalmia - esophageal atresia
Autosomal dominant centronuclear myopathy
Autosomal dominant limb-girdle muscular dystrophy type 1A
Autosomal dominant secondary polycythemia
B-cell chronic lymphocytic leukemia
Benign paroxysmal torticollis of infancy
Brugada syndrome
COFS syndrome
Chronic myeloid leukemia
Colobomatous microphthalmia
Combined immunodeficiency due to STK4 deficiency
Dedifferentiated liposarcoma
Dentatorubral pallidoluysian atrophy
Essential thrombocythemia
Familial melanoma
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Familial thoracic aortic aneurysm and aortic dissection
Fibronectin glomerulopathy
Giant cell glioblastoma
Gliosarcoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inherited acute myeloid leukemia
Isolated anophthalmia - microphthalmia
Laron syndrome with immunodeficiency
Li-Fraumeni syndrome
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Monomelic amyotrophy
Multiple paragangliomas associated with polycythemia
Myotilin-related myofibrillar myopathy without spheroid body
Nager syndrome
Odontoleukodystrophy
Papilloma of choroid plexus
Pontocerebellar hypoplasia type 1
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Septo-optic dysplasia
Spheroid body myopathy
Spinocerebellar ataxia type 19 / 22
Spinocerebellar ataxia type 6
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Translocation renal cell carcinoma
Well-differentiated liposarcoma
Wolf-Hirschhorn syndrome
Xeroderma pigmentosum complementation group G
Partial pancreatic agenesis
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis
Kallmann syndrome
Neurologic Waardenburg-Shah syndrome
Paris-Trousseau thrombocytopenia
Peripheral primitive neuroectodermal tumor
Waardenburg syndrome type 2
Waardenburg-Shah syndrome
Action myoclonus - renal failure syndrome
Autosomal recessive malignant osteopetrosis
Autosomal recessive optic atrophy, OPA7 type
Cap myopathy
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Digitotalar dysmorphism
Gaucher disease type 1
Kostmann syndrome
Sheldon-Hall syndrome
Trismus - pseudocamptodactyly
Typical nemaline myopathy
Unverricht-Lundborg disease
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.