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DO Term : focal segmental glomerulosclerosis 5 [DOID:0111130] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the INF2 gene on chromosome 14q32.33.
  • synonyms:
  • ICD10CM:N04.1,
  • OMIM:613237,
  • FSGS5,
  • 613237,
  • MESH:C567687
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