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DO Term : focal segmental glomerulosclerosis 9 [DOID:0111134] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A focal segmental glomerulosclerosis that has_material_basis_in an autosomal recessive mutation of the CRB2 gene on chromosome 9q33.3.

synonyms:
OMIM:616220,
ICD10CM:N04.1,
FSGS9,
616220

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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