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| Ataxia and cerebellar anomalies - narrow panel v0.5 | PEX16 |
Ellen McDonagh gene: PEX16 was added gene: PEX16 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: PEX16 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PEX16 were set to Zellweger syndrome (614876); Peroxisome biogenesis disorder 8B (#614877) infantile progressive ataxia and spastic paresis |
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