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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Isolated focal cortical dysplasia type IIb
Childhood-onset nemaline myopathy

TSC1 ACTA1
KBTBD13
KLHL41
NEB
TPM2
TPM3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TSC1
(0.55)
ACTA1



Citations in the biomedical literature:


Isolated focal cortical dysplasia type IIb
TSC1
Childhood-onset nemaline myopathy
ACTA1 KBTBD13 KLHL41 NEB TPM2 TPM3



Isolated focal cortical dysplasia type IIb
Childhood-onset nemaline myopathy

Synonym(s):
- FCD type IIb

Synonym(s):
- Mild nemaline myopathy

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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 -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.