peroxisome biogenesis disorder 12A

Summary
Synonym
  • peroxisome biogenesis disorder 12A (Zellweger)
Definition
A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX19 gene on chromosome 1q23.
Super Class
Zellweger syndrome
Disease Ontology
DOID:0080486
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5824 PEX19 peroxisomal biogenesis factor 19

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024