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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.

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Sub-types

Retinitis pigmentosa 59 (0)

Broader categories

Disease (618) Hereditary disease (172) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of glycosylation (0)

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: PHASE1 • Sponsor: Eva Morava-Kozicz • Aim: Disease control

Last updated Jun 27, 2026 14:01 UTC