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Intermediate nemaline myopathy

4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Hereditary site-specific ovarian cancer syndrome

2 associated genes
No signs/symptoms info

Intermediate nemaline myopathy

Hereditary site-specific ovarian cancer syndrome

ACTA1	(UniProt - OMIM)		BRCA1	(UniProt - OMIM)
KLHL41	(UniProt - OMIM)		BRCA2	(UniProt - OMIM)
NEB	(UniProt - OMIM)
TPM3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TPM3	(0.63)	BRCA1

Citations in the biomedical literature:

Intermediate nemaline myopathy		Hereditary site-specific ovarian cancer syndrome

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.