Zellweger Syndrome Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	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. (Human Disease Ontology, DOID_905)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D015211
Similar Terms
Downloads & Tools

Genes

14 genes/proteins associated with the disease Zellweger Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
HSD17B4	hydroxysteroid (17-beta) dehydrogenase 4	2.88009
PEX6	peroxisomal biogenesis factor 6	2.88009
PEX5	peroxisomal biogenesis factor 5	2.88009
PEX2	peroxisomal biogenesis factor 2	2.88009
PEX3	peroxisomal biogenesis factor 3	2.88009
PEX1	peroxisomal biogenesis factor 1	2.88009
PEX16	peroxisomal biogenesis factor 16	2.88009
PEX14	peroxisomal biogenesis factor 14	2.88009
PEX13	peroxisomal biogenesis factor 13	2.88009
PEX10	peroxisomal biogenesis factor 10	2.88009
PEX19	peroxisomal biogenesis factor 19	2.88009
PEX26	peroxisomal biogenesis factor 26	2.88009
ABCD3	ATP-binding cassette, sub-family D (ALD), member 3	2.88009
PEX12	peroxisomal biogenesis factor 12	2.88009