Search Ontology:
Human Disease
nephrotic syndrome type 17
- Term ID
- DOID:0080392
- Synonyms
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- Definition
- A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/30179222
- References
- Ontology
- Human Disease ( DOID:0080392 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models