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DO Term : nephrotic syndrome type 10 [DOID:0080386] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13.

synonyms:
615861,
OMIM:615861

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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