Nephrotic Syndrome - WT1 Associated

Preferred Label : Nephrotic Syndrome - WT1 Associated;

NCIt definition : Nephrotic syndrome attributed to mutation(s) in the WT1 gene.;

Origin ID

C123106;

UMLS CUI

C4054361;

Has associated anatomic sites
- Genitourinary System [NCIt concept]
- Kidney [NCIt concept]
- Urinary System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Nephrology Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Genitourinary System [NCIt concept]
- Kidney [NCIt concept]
- Urinary System [NCIt concept]
disease_mapped_to_gene
- WT1 Gene [NCIt concept]
related_to_genetic_biomarker
- WT1 Gene [NCIt concept]