ODCs

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2 OMIM references -
1 associated gene
6 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 4

1 OMIM reference -
1 associated gene
5 signs/symptoms

Familial multiple trichoepithelioma

Familial cylindromatosis

CYLD

Citations in the biomedical literature:

Familial multiple trichoepithelioma		Familial cylindromatosis
	Synonym(s): (no synonyms)		Synonym(s): - Turban tumor syndrome

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare oncologic disease - Rare skin disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 2 OMIM references - 1 MeSH reference: C536552		External references: 1 OMIM reference - 1 MeSH reference: C536611


COMMON SIGNS	- Autosomal dominant inheritance - Skin tumors / lumps / epidermal cysts - Subcutaneous nodules / lipomas / tumefaction / swelling - Telangiectasiae of the skin

Familial multiple trichoepithelioma		Familial cylindromatosis
	Very frequent - Follicular / erythematous / edematous papules / milium Occasional - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma)		Very frequent - Scalp cyst / giant nevus