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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models