Nephrotic Syndrome Type 14
Disease ID: disease_node_19090
Connections displayed (default: 10).
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| Dbxref | MIM:617575 |
|---|---|
| Subclassof | DOID_2590, DOID_0050737 |
| Data Source | DOID |
| Doid Label | nephrotic syndrome type 14 |
| Doid Description | 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19090 |
| Doid Id | DOID_0080265 |
| Label | Nephrotic Syndrome Type 14 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)