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DOID:905 - Zellweger syndrome
Disease Ontology Definition:A peroxisomal disease that is characterized by the reduction or absence of functional peroxisomes in the cells of an individual that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes.
Synonyms: cerebrohepatorenal syndrome , congenital iron overload, peroxisome biogenesis disorder,
Echinobase Genes
:
pex1
| OMIM:214100 - peroxisome biogenesis disorder 1a (zellweger); pbd1a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
peroxisomal disease (is_a)