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Human Disease

focal segmental glomerulosclerosis 5

Term ID
DOID:0111130
Synonyms
  • FSGS5
Definition
A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the INF2 gene on chromosome 14q32.33. https://www.ncbi.nlm.nih.gov/pubmed/20023659
References
Ontology
Human Disease   ( DOID:0111130 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models