Cytoscape Web
Click node...


1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
17q11 microdeletion syndrome
Familial rhabdoid tumor

NF1 SMARCA4
RNF135 SMARCB1
SUZ12


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NF1
(0.63)
SMARCA4



Citations in the biomedical literature:


17q11 microdeletion syndrome
NF1 RNF135 SUZ12
Familial rhabdoid tumor
SMARCA4 SMARCB1



17q11 microdeletion syndrome
Familial rhabdoid tumor

Synonym(s):
- Del(17)(q11)
- Monosomy 17q11
- NF1 microdeletion syndrome
- Neurofibromatosis type 1 microdeletion syndrome

Synonym(s):
- RTPS
- Rhabdoid tumor predisposition syndrome

Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease

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

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: autosomal dominant

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

No signs/symptoms info available.