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

Autism spectrum disorder-epilepsy-arthrogryposis syndrome

SLC35A2-CDG


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC35A3	(0.73)	SLC35A2

Citations in the biomedical literature:

Autism spectrum disorder-epilepsy-arthrogryposis syndrome		SLC35A2-CDG
	Synonym(s): - SLC35A3-CDG		Synonym(s): - CDG syndrome type 2m - CDG syndrome type IIm - CDG-IIm - CDG2M - Congenital disorder of glycosylation type 2m - Congenital disorder of glycosylation type IIm

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: unknown

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

No signs/symptoms info available.