Nephrotic Syndrome Type 5
Disease ID: disease_node_19086
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| Dbxref | MIM:614199 |
|---|---|
| Subclassof | DOID_2590, DOID_0050737 |
| Data Source | DOID |
| Synonyms | nephrotic syndrome type 5, with or without ocular abnormalities |
| Doid Label | nephrotic syndrome type 5 |
| Doid Description | A familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19086 |
| Doid Id | DOID_0080380 |
| Label | Nephrotic Syndrome Type 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)