FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Holt-Oram syndrome ID (Ontology) DOID:0060468 (Human Disease)
Definition A syndrome characterized by congenital anomalies located_in heart and located_in upper limb.
Also Known As "atrio-digital syndrome" ; "atriodigital dysplasia" ; "heart-hand 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)
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
 Holt-Oram syndrome       1
 for disease ribbon | Holt-Oram syndrome       1
 model of | Holt-Oram syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Holt-Oram syndrome  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "atrio-digital syndrome" EXACT
    "atriodigital dysplasia" EXACT
    "heart-hand syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:6666
ICD10CM:Q87.2
MESH:C535326
MIM:142900
NCI:C125592
ORDO:392
SNOMEDCT_US_2023_03_01:205814003
UMLS_CUI:C0265264