Zellweger spectrum disorders
MONDO:0019609The most severe variant seen in the peroxisome biogenesis disorders that is characterized by neuronal migration defects in the brain, dysmorphic craniofacial features, profound hypotonia, neonatal seizures, and liver dysfunction.
Also known as: ZS, ZWS, Zellweger spectrum disorders, Zellweger syndrome, cerebrohepatorenal syndrome, Zellweger leukodystrophy
14 clinical trials for this condition and its sub-types, 6 tagged with Zellweger spectrum disorders itself.
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Browse by category →Sub-types of Zellweger spectrum disorders
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Peroxisome biogenesis disorder due to PEX1 defect 0 trials · 1 incl. sub-types
2 sub-types
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Peroxisome biogenesis disorder 9B 0 trials
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2 sub-types
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1 sub-type
- Peroxisome biogenesis disorder 14B 0 trials
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3 sub-types
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2 sub-types
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2 sub-types
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2 sub-types
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1 sub-type
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2 sub-types
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2 sub-types
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2 sub-types
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2 sub-types
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2 sub-types