Cytoscape Web
Click node...

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Gräsbeck-Imerslund disease
1 OMIM reference -
2 associated genes
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Gräsbeck-Imerslund disease

CBL
(UniProt - OMIM)
 AMN
(UniProt - OMIM)
CUBN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CBL
(0.49)
CUBN


Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Gräsbeck-Imerslund disease
AMN CUBN



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Gräsbeck-Imerslund disease

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML
Synonym(s):
- Familial megaloblastic anemia
- Selective cobalamin malabsorption with proteinuria
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare gastroenterologic disease
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.