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DO Term : nephrotic syndrome type 19 [DOID:0080394] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial nephrotic syndrome that has_material_basis_in compound heterozygous mutation in the NUP160 gene on chromosome 11p11.

synonyms:
OMIM:618178,
618178

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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