ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
6 signs/symptoms

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

Familial multiple trichoepithelioma


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

Citations in the biomedical literature:

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy		Familial multiple trichoepithelioma
	Synonym(s): - Progressive neurosensory deafness - hypertrophic cardiomyopathy - Progressive neurosensory hearing loss - hypertrophic cardiomyopathy - Progressive sensorineural deafness - hypertrophic cardiomyopathy		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C536552

Familial multiple trichoepithelioma
	Very frequent - Autosomal dominant inheritance - Follicular / erythematous / edematous papules / milium - Skin tumors / lumps / epidermal cysts - Subcutaneous nodules / lipomas / tumefaction / swelling Frequent - Telangiectasiae of the skin Occasional - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma)
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
(no data available)