Cytoscape Web
Click node...


2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
6 signs/symptoms
Anaplastic ependymoma
5q35 microduplication syndrome

C11ORF95 NSD1
RELA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RELA
(0.63)
NSD1



Citations in the biomedical literature:


Anaplastic ependymoma
C11ORF95 RELA
5q35 microduplication syndrome
NSD1



Anaplastic ependymoma
5q35 microduplication syndrome

Synonym(s):
- High-grade ependymoma

Synonym(s):
- Dup(5)(q35)
- Trisomy 5q35

Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

5q35 microduplication syndrome

Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Microcephaly
- Short stature / dwarfism / nanism

Frequent
- Delayed bone age
- Myopia
- Psychic / behavioural troubles



Anaplastic ependymoma

(no data available)