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🔗 CustomizeMedical Overview of Congenital Disorder Of Glycosylation Type Ir
Sources citedDDOST-CDG is a form of congenital disorders of N-linked glycosylation characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction. The disease is caused by mutations in the gene <i> DDOST </i> (1p36.1).
Classification & codes: GARD 0012398 · Orphanet ORPHA:300536 · OMIM 614507 · ICD-10 E77.8
Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.
News & Updates
ALYFTREK shows positive Phase 3 results in children ages 2–5
Vertex plans global regulatory submissions for this pediatric age group in the first half of 2026.
Airway clearance routines that actually work for teens
3 open trials match this profile
Locations in NC, FL and GA.
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Disclosure, accommodations, insurance transitions and workplace planning for teens and young adults with CDG1R.
Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.