OBO ID: DOID:0111130 |
Term Name: | focal segmental glomerulosclerosis 5 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0111130 ) |
OTHER focal segmental glomerulosclerosis 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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