| Term Name: | RENI syndrome |
|---|---|
| Synonyms: | nephrotic syndrome type 14 |
| Definition: | A familial nephrotic syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the sphingosine-1-phosphate lyase 1 (SGPL1) gene on chromosome 10q21. |
| Ontology: | Human Disease [DOID:0080265] ( DOID:0080265 ) |