Huppke-Brendel syndrome

MONDO:0013772

Also known as: Huppke-Brendel syndrome, acetyl CoA transporter deficiency, congenital cataract-deafness-severe developmental delay syndrome, congenital cataracts, hearing loss, and neurodegeneration, lethal neurodegenerative disorder due to copper transport defect, CCHLND

0 clinical trials for this condition and its sub-types, 0 tagged with Huppke-Brendel syndrome itself.

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↑ Hereditary disease (18187)

Including sub-types (0) Tagged with Huppke-Brendel syndrome (0)

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