OBO ID: DOID:0080384 |
Term Name: | nephrotic syndrome type 6 | Search Ontology: | |
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Definition: | A familial nephrotic syndrome that has_material_basis_in homozygous mutation in the PTPRO gene on chromosome 12p12. https://www.ncbi.nlm.nih.gov/pubmed/21722858 | ||
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Ontology: | Human Disease ( DOID:0080384 ) |
OTHER nephrotic syndrome type 6 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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