Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

CBL CSF1R


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CBL
(0.96)
CSF1R



Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
CSF1R



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML

Synonym(s):
- ALSP
- Autosomal dominant leukoencephalopathy with neuroaxonal spheroids
- HDLS
- Hereditary diffuse leukoencephalopathy with spheroids
- POLD
- Pigmentary orthochromatic leukodystrophy

Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic 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: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.