Search Ontology:
Human Disease
nephrotic syndrome type 13
- Term ID
- DOID:0080381
- Synonyms
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- Definition
- A familial nephrotic syndrome characterized by early onset of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis that has_material_basis_in homozygous mutation in the NUP205 gene on chromosome 7q33. https://www.ncbi.nlm.nih.gov/pubmed/26878725
- References
- Ontology
- Human Disease ( DOID:0080381 )
- is a type of
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Genes Involved
Zebrafish Models