Search Ontology:
Human Disease
nephrotic syndrome type 6
- Term ID
- DOID:0080384
- Synonyms
-
- 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
- References
- Ontology
- Human Disease ( DOID:0080384 )
- is a type of
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