Global Variome shared LOVD

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Phenotype #0000250423 Individual ID 00332236 Associated disease ? Diagnosis/Initial nephrotic syndrome, neurologic disease Diagnosis/Definite - Phenotype details 2y2m-onset renal disease; 3y-onset end-stage renal disease; steroid-resistant nephrotic syndrome; biopsy focal segmental glomerulosclerosis; 7.5y-transplant, transplant rejection; 2.2y-onset developmental delay; 4.5y-onset epilepsy; epilepsy, global developmental delay, mild cerebral and cerebellar atrophy Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-02-15 21:39:28 +01:00 (CET) Date last edited N/A

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