WormBase Tree Display for DO_term: DOID:0080380
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DOID:0080380 | Name | nephrotic syndrome type 5 | |||
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Status | Valid | ||||
Definition | 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. | ||||
Synonym | Exact | nephrotic syndrome type 5, with or without ocular abnormalities | |||
Parent | Is_a | DOID:2590 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 614199 | |
Attribute_of | Gene_by_orthology | WBGene00002247 |