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Gardner syndrome

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

PROTEIN INTERACTIONS: 1

Typical nemaline myopathy

5 associated genes
No signs/symptoms info

Gardner syndrome

Typical nemaline myopathy

APC	(UniProt - OMIM)		ACTA1	(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)	APC	(0.63)	NEB

Citations in the biomedical literature:

Gardner syndrome		Typical nemaline myopathy

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease - Rare skin disease		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: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.