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DO Term : peroxisome biogenesis disorder 10A [DOID:0080484] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX3 gene on chromosome 6q24.

synonyms:
OMIM:614882,
peroxisome biogenesis disorder 10A (Zellweger),
614882

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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