ODCs

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1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

4 OMIM references -
3 associated genes
No signs/symptoms info

Sebocystomatosis

Male infertility with normal virilization due to meiosis defect


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT17	(0.63)	CFTR

Citations in the biomedical literature:

Sebocystomatosis		Male infertility with normal virilization due to meiosis defect
	Synonym(s): - Steatocystoma multiplex		Synonym(s): - Azoospermia due to maturation arrest - Azoospermia due to meiosis defect - Male infertility with normal virilization due to maturation arrest

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

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 4 OMIM references - No MeSH references

Sebocystomatosis
	Very frequent - Adenoma sebaceum - Autosomal dominant inheritance - Skin tumors / lumps / epidermal cysts Occasional - Urinary / renal lithiasis / kidney stones / nephritic colic
Male infertility with normal virilization due to meiosis defect
(no data available)