Search Ontology:
Human Disease
focal segmental glomerulosclerosis 5
- Term ID
- DOID:0111130
- Synonyms
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- 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
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- ICD10CM:N04.1
- MESH:C567687
- MIM:613237
- Ontology
- Human Disease ( DOID:0111130 )
- is a type of
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Genes Involved
Zebrafish Models