ODCs

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

PROTEIN INTERACTIONS: 1

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

DDOST-CDG

Adult-onset proximal spinal muscular atrophy, autosomal dominant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DDOST	(0.63)	VAPB

Citations in the biomedical literature:

DDOST-CDG		Adult-onset proximal spinal muscular atrophy, autosomal dominant
	Synonym(s): - CDG syndrome type Ir - CDG-Ir - CDG1R - Carbohydrate deficient glycoprotein syndrome type Ir - Congenital disorder of glycosylation type 1r - Congenital disorder of glycosylation type Ir		Synonym(s): - Finkel disease

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease - Rare neurologic 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: unknown		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood 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.