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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Testicular seminomatous germ cell tumor

CBL DNAAF1
KITLG
SPRY4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CBL
(0.79)
SPRY4



Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Testicular seminomatous germ cell tumor
DNAAF1 KITLG SPRY4



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Testicular seminomatous germ cell tumor

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

Synonym(s):
- Dysgerminoma of the testis
- Dysgerminomatous germ cell tumor of the testis
- Seminoma of the testis
- Seminomatous germ cell tumor of the testis
- Testicular dysgerminoma
- Testicular dysgerminomatous germ cell tumor
- Testicular seminoma

Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare oncologic disease
- Rare urogenital 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: any age
Type of inheritance: sporadic

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

No signs/symptoms info available.