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Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy

MONDO:0030835

Also known as: DIGFAN

1 clinical trial for this condition and its sub-types.

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Disease (679) Hereditary disease (176) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)
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  • Gene study aims to decode rare nerve disorder variations

    Knowledge-focused Recruiting now

    This study looks at how different mutations in the MORC2 gene lead to different symptoms, from Charcot-Marie-Tooth disease to a more complex condition called DIFGAN. Researchers will collect skin and blood samples from 45 participants to measure epigenetic and genetic markers. Th…

    Sponsor: Hospices Civils de Lyon • Aim: Knowledge-focused

    Last updated Jun 27, 2026 14:00 UTC

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