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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Congenital mesoblastic nephroma
Severe congenital nemaline myopathy

ETV6 ACTA1
NTRK3 KLHL40
KLHL41
NEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ETV6
(0.55)
ACTA1



Citations in the biomedical literature:


Congenital mesoblastic nephroma
ETV6 NTRK3
Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB



Congenital mesoblastic nephroma
Severe congenital nemaline myopathy

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive

External references:
No OMIM references
1 MeSH reference: D018201
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.