FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term acheiropody ID (Ontology) DOID:0050603 (Human Disease)
Definition An osteochondrodysplasia characterized by a lack of formation of the distal extremities has_material_basis_in mutation in the LMBR1 gene.
Also Known As "Acheiropodia" ; "Horn-Kolb 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
 acheiropody       1
 for disease ribbon | acheiropody       1
 model of | acheiropody       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
bone development disease         |
 |__osteochondrodysplasia________|
cartilage disease                |
 |__osteochondrodysplasia________|
                                 acheiropody  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
osteochondrodysplasia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Acheiropodia" EXACT
    "Horn-Kolb Syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:376
MIM:200500