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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Dedifferentiated liposarcoma
ALDH18A1-related De Barsy syndrome

CDK4 ALDH18A1
HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MDM2
(0.63)
ALDH18A1



Citations in the biomedical literature:


Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2
ALDH18A1-related De Barsy syndrome
ALDH18A1



Dedifferentiated liposarcoma
ALDH18A1-related De Barsy syndrome

Synonym(s):
- DDLS

Synonym(s):
- Delta-1-pyrroline 5-carboxylate synthetase deficiency
- Neurocutaneous syndrome, Bicknell type
- P5CS deficiency

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare skin disease
- Rare surgical thoracic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal recessive

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

ALDH18A1-related De Barsy syndrome

Very frequent
- Cataract / lens opacification
- Hyperelastic skin / cutaneous hyperlaxity
- Hyperextensible joints / articular hyperlaxity
- Intellectual deficit / mental / psychomotor retardation / learning disability



Dedifferentiated liposarcoma

(no data available)