ODCs

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

COMMON GENES: 1

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

Familial multinodular goiter

Pleuropulmonary blastoma family tumor susceptibility syndrome

Citations in the biomedical literature:

Familial multinodular goiter		Pleuropulmonary blastoma family tumor susceptibility syndrome
	Synonym(s): - FMNG - Familial MNG		Synonym(s): - DICER1 syndrome - PPB family tumor susceptibility syndrome - PPBFTDS - Pleuro-pulmonary blastoma family tumor susceptibility syndrome

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare oncologic disease - Rare respiratory disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		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: 1 OMIM reference - No MeSH references

No signs/symptoms info available.