FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term autosomal dominant tubulointerstitial kidney disease 4 ID (Ontology) DOID:0061119 (Human Disease)
Definition An autosomal dominant tubulointerstitial kidney disease characterized by early-onset anemia and increased serum uric acid with a bland urinalysis and without proteinuria that has_material_basis_in heterozygous mutation in the renin gene on chromosome 1q32.
Also Known As "familial juvenile hyperuricemic nephropathy 2"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 autosomal dominant tubulointerstitial kidney disease 4       1
 for disease ribbon | autosomal dominant tubulointerstitial kidney disease 4       1
 model of | autosomal dominant tubulointerstitial kidney disease 4       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal dominant disease__
kidney disease______________|
                            autosomal dominant tubulointerstitial kidney disease
                             |__autosomal dominant tubulointerstitial kidney disease 4  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant tubulointerstitial kidney disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "familial juvenile hyperuricemic nephropathy 2" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:613092
ORDO:217330