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Typical nemaline myopathy

5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Gardner syndrome

1 OMIM reference -
1 associated gene
No signs/symptoms info

Typical nemaline myopathy

Gardner syndrome

ACTA1	(UniProt - OMIM)		APC	(UniProt - OMIM)
CFL2	(UniProt - OMIM)
KLHL41	(UniProt - OMIM)
NEB	(UniProt - OMIM)
TPM2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NEB	(0.63)	APC

Citations in the biomedical literature:

Typical nemaline myopathy		Gardner syndrome

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease - Rare skin disease

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D005736

No signs/symptoms info available.