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DO Term : focal segmental glomerulosclerosis 7 [DOID:0111132] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the PAX2 gene on chromosome 10q24.31.

synonyms:
OMIM:616002,
FSGS7,
ICD10CM:N04.1,
616002

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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