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Peroxisome Biogenesis Disorder 3B

Disease ID: disease_node_17526

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DbxrefMIM:266510
SubclassofDOID_0080377, DOID_0050737
Data SourceDOID
Doid Labelperoxisome biogenesis disorder 3B
Doid DescriptionA peroxisome biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_17526
Doid IdDOID_0081241
LabelPeroxisome Biogenesis Disorder 3B