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DO Term : focal segmental glomerulosclerosis 6 [DOID:0111131] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A focal segmental glomerulosclerosis that has_material_basis_in an autosomal recessive mutation of the MYO1E gene on chromosome 15q22.2.

synonyms:
ICD10CM:N04.1,
OMIM:614131,
FSGS6,
614131

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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