Cytoscape Web
Click node...

Kleefstra syndrome due to a point mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Dedifferentiated liposarcoma
3 associated genes
No signs/symptoms info
Kleefstra syndrome due to a point mutation
Dedifferentiated liposarcoma

EHMT1
(UniProt - OMIM)
 CDK4
(UniProt - OMIM)
HMGA2
(UniProt - OMIM)
MDM2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EHMT1
(0.63)
MDM2


Citations in the biomedical literature:


Kleefstra syndrome due to a point mutation
EHMT1
Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2



Kleefstra syndrome due to a point mutation
Dedifferentiated liposarcoma

Synonym(s):
(no synonyms)

Synonym(s):
- DDLS
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.