FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term trichorhinophalangeal syndrome type III ID (Ontology) DOID:0080376 (Human Disease)
Definition A syndrome that is characterized by sparse hair, beaked nose, long upper lip, and severe metacarpophalangeal shortening and has_material_basis_in heterozygous mutation in the TRPS1 gene on chromosome 8q23.
Also Known As "trichorhinophalangeal syndrome type 3"
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
 trichorhinophalangeal syndrome type III       1
 for disease ribbon | trichorhinophalangeal syndrome type III       1
 model of | trichorhinophalangeal syndrome type III       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                trichorhinophalangeal syndrome type III  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
  • "trichorhinophalangeal syndrome type 3" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:190351
ORDO:77258