FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term papilledema ID (Ontology) DOID:146 (Human Disease)
Definition
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
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
 for disease ribbon | acrodysostosis       2
 for disease ribbon | diastrophic dysplasia       1
 for disease ribbon | galactokinase deficiency       1
 for disease ribbon | Johanson-Blizzard syndrome       1
 for disease ribbon | multiple intestinal atresia       1
 for disease ribbon | Smith-Lemli-Opitz syndrome       1
 for disease ribbon | thrombocytopenia-absent radius syndrome       1
 model of | acrodysostosis       2
 model of | diastrophic dysplasia       1
 model of | galactokinase deficiency       1
 model of | Johanson-Blizzard syndrome       1
 model of | multiple intestinal atresia       1
 model of | Smith-Lemli-Opitz syndrome       1
 model of | thrombocytopenia-absent radius syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
  cranial nerve disease
   |__optic nerve disease
       |__papilledema
           |__Foster-Kennedy syndrome
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a optic nerve disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
GARD:7318
ICD10CM:H47.1
ICD9CM:377.0
MESH:D010211
NCI:C3307
SNOMEDCT_US_2023_03_01:423488006
UMLS_CUI:C0030353