ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Familial cylindromatosis

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CYLD	(0.76)	MYO6

Citations in the biomedical literature:

Familial cylindromatosis		Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
	Synonym(s): - Turban tumor syndrome		Synonym(s): - Progressive neurosensory deafness - hypertrophic cardiomyopathy - Progressive neurosensory hearing loss - hypertrophic cardiomyopathy - Progressive sensorineural deafness - hypertrophic cardiomyopathy

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C536611		External references: 1 OMIM reference - No MeSH references

Familial cylindromatosis
	Very frequent - Autosomal dominant inheritance - Scalp cyst / giant nevus - Skin tumors / lumps / epidermal cysts - Subcutaneous nodules / lipomas / tumefaction / swelling - Telangiectasiae of the skin
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
(no data available)