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Echinobase
Summary Literature (0)
DOID:0080483 - peroxisome biogenesis disorder 8A

Disease Ontology Definition:A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX16 gene on chromosome 11p11.

Synonyms: peroxisome biogenesis disorder 8A (Zellweger),

Echinobase Genes : pex16


OMIM:
MIM:614876 - peroxisome biogenesis disorder 8a (zellweger); pbd8a peroxisome biogenesis disorder, complementation group 9, included; cg9, included;; peroxisome biogenesis disorder, complementation group d, included; cgd, included

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): peroxisomal biogenesis disorder (is_a)