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Dedifferentiated liposarcoma

3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Oxoglutaricaciduria

1 OMIM reference -
1 associated gene
10 signs/symptoms

Dedifferentiated liposarcoma

Oxoglutaricaciduria

CDK4	(UniProt - OMIM)		OGDH	(UniProt - OMIM)
HMGA2	(UniProt - OMIM)
MDM2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MDM2	(0.63)	OGDH

Citations in the biomedical literature:

Dedifferentiated liposarcoma		Oxoglutaricaciduria
	Synonym(s): - DDLS		Synonym(s): - Alpha-ketoglutarate dehydrogenase deficiency

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: adult Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536582

Oxoglutaricaciduria
	Very frequent - Ataxia / incoordination / trouble of the equilibrium - Autosomal recessive inheritance - Hypertonia / spasticity / rigidity / stiffness - Intellectual deficit / mental / psychomotor retardation / learning disability - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Organic acid metabolism anomalies - Short stature / dwarfism / nanism Frequent - Anomaly / ectopia / hypoplasia / atresia of salivary glands / salivary duct - Hydrocephaly - Movement disorder
Dedifferentiated liposarcoma
(no data available)