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DO Term : focal segmental glomerulosclerosis 3 [DOID:0112245] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A focal segmental glomerulosclerosis that has_material_basis_in loss of function mutation in the CD2AP gene on chromosome 6p12.3.
  • synonyms:
  • OMIM:607832,
  • 607832,
  • FSGS3
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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