ODCs

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

PROTEIN INTERACTIONS: 2

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

Familial multinodular goiter

Proximal spinal muscular atrophy type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DICER1 DICER1	(0.63) (0.63)	SMN1 SMN2

Citations in the biomedical literature:

Familial multinodular goiter		Proximal spinal muscular atrophy type 1
	Synonym(s): - FMNG - Familial MNG		Synonym(s): - Infantile spinal muscular atrophy - SMA-I - SMA1 - Werdnig-Hoffmann disease

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	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: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.