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DHDDS-CDG

MONDO:1040054

Any congenital disorder of glycosylation caused by variants in the DHDDS gene.

Also known as: DHDDS-CDG

1 clinical trial for this condition and its sub-types, 1 tagged with DHDDS-CDG itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18187) ↑ Disorder of glycosylation (74)

Sub-types of DHDDS-CDG

Retinitis pigmentosa 59 0 trials

Including sub-types (1) Tagged with DHDDS-CDG (1)

Trials to join now! 1

Could a common supplement help a rare disease? early trial begins

Disease control Recruiting now

This early-stage trial is testing the safety of a dietary supplement called NMN in 8 people with a rare genetic disorder known as DHDDS-CDG, which affects movement and development. Participants will take 250 mg of NMN daily for 6 months, with an optional 12-month follow-up. The m…

Phase 1 • Sponsor: Eva Morava-Kozicz • Aim: Disease control

Last updated Jun 27, 2026 14:01 UTC