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DO Term : peroxisome biogenesis disorder 3A [DOID:0080478] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17.

synonyms:
614859,
OMIM:614859,
peroxisome biogenesis disorder 3A (Zellweger)

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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