Congenital disorder of glycosylation type 2G

Symptoms of Congenital disorder of glycosylation type 2G

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Genetics of Congenital disorder of glycosylation type 2G

Modes of inheritance: Autosomal recessive inheritance (HPO, OMIM, Orphanet) ...Source: GTR (NCBI/NIH)1 ...

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Names and Terminology

Synonyms: CDG 2G ; CDG IIg ; CDGII/COG1 CEREBROCOSTOMANDIBULAR-LIKE SYNDROME ; COG1-CDG (CDG-IIg) ; CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg ...Source: GTR (NCBI/NIH)2 ...

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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C1970016/ 
  2. ibid.

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