Nephrotic Syndrome - LMX1B Associated

Preferred Label : Nephrotic Syndrome - LMX1B Associated;

Alternative definition : NICHD: Nephrotic syndrome attributed to mutation(s) in the LMX1B gene.;

Détails

Origin ID

C123090;

UMLS CUI

C4054378;

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
- 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
- LMX1B Gene [NCIt concept]
related_to_genetic_biomarker
- LMX1B Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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