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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Fibrosarcoma
Childhood-onset nemaline myopathy

ETV6 ACTA1
NTRK3 KBTBD13
KLHL41
NEB
TPM2
TPM3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Fibrosarcoma
ETV6 NTRK3
Childhood-onset nemaline myopathy
ACTA1 KBTBD13 KLHL41 NEB TPM2 TPM3



Fibrosarcoma
Childhood-onset nemaline myopathy

Synonym(s):
(no synonyms)

Synonym(s):
- Mild nemaline myopathy

Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

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 -
1 MeSH reference: D005354
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.