OBO ID: DOID:0080393 |
Term Name: | nephrotic syndrome type 18 | Search Ontology: | |
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Definition: | A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42. https://www.ncbi.nlm.nih.gov/pubmed/30179222 | ||
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Ontology: | Human Disease ( DOID:0080393 ) |
OTHER nephrotic syndrome type 18 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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