FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term FG syndrome ID (Ontology) DOID:14711 (Human Disease)
Definition A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern.
Also Known As "Keller syndrome" ; "Opitz-Kaveggia syndrome"
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)
Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 FG syndrome       4      1
 for disease ribbon | FG syndrome       4       --
 model of | FG syndrome       4       --
Spanning Tree (Parents/Children)
Only view relationship: 
X-linked monogenic disease
 |__X-linked recessive disease__
disease                         |
 |__syndrome____________________|
                                FG syndrome  5 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a X-linked recessive disease
syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Keller syndrome" EXACT
    "Opitz-Kaveggia syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:2317
MESH:C537923
MIM:300321
MIM:300406
MIM:300422
MIM:300581
MIM:305450
ORDO:323
ORDO:93932
SNOMEDCT_US_2023_03_01:49984004
UMLS_CUI:C0220769