ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Familial multinodular goiter

Anauxetic dysplasia

DICER1	(UniProt - OMIM)		POP1	(UniProt - OMIM)
			RMRP	(OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DICER1	(0.63)	POP1

Citations in the biomedical literature:

Familial multinodular goiter		Anauxetic dysplasia
	Synonym(s): - FMNG - Familial MNG		Synonym(s): - Spondyloepimetaphyseal dysplasia, Menger type - Spondyloepimetaphyseal dysplasia, anauxetic type

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: - Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538256

No signs/symptoms info available.