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DO Term : nephrotic syndrome type 6 [DOID:0080384] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial nephrotic syndrome that has_material_basis_in homozygous mutation in the PTPRO gene on chromosome 12p12.

synonyms:
614196,
OMIM:614196

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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