FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term sialuria ID (Ontology) DOID:3659 (Human Disease)
Definition A lysosomal storage disease characterized by increased sialic acid in the urine.
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
 sialuria      20
 for disease ribbon | sialuria      20
 model of | sialuria      20
Spanning Tree (Parents/Children)
Only view relationship:
  inherited metabolic disorder
   |__lysosomal storage disease
       |__sialuria  20 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a lysosomal storage disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
MESH:D029461
MIM:269921
MIM:604369
NCI:C85067
SNOMEDCT_US_2023_03_01:238051008
UMLS_CUI:C0342853