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Well-differentiated liposarcoma
3 associated genes
4 signs/symptoms
PROTEIN INTERACTIONS: 1
Pyruvate carboxylase deficiency, severe neonatal type
1 associated gene
No signs/symptoms info
Well-differentiated liposarcoma
Pyruvate carboxylase deficiency, severe neonatal type

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

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


Citations in the biomedical literature:


Well-differentiated liposarcoma
CDK4 HMGA2 MDM2
Pyruvate carboxylase deficiency, severe neonatal type
PC



Well-differentiated liposarcoma
Pyruvate carboxylase deficiency, severe neonatal type

Synonym(s):
- ALT
- Atypical lipoma
- Atypical lipomatous tumor
- WDLS
Synonym(s):
- Pyruvate carboxylase deficiency type B
Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic 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: -
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:
No OMIM references
No MeSH references
Well-differentiated liposarcoma

Very frequent
- Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma
- Subcutaneous nodules / lipomas / tumefaction / swelling

Occasional
- Functional anomalies of the kidney and the urinary tract
- Intestinal transit disorder


Pyruvate carboxylase deficiency, severe neonatal type

(no data available)