FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term distal arthrogryposis type 7 ID (Ontology) DOID:0111603 (Human Disease)
Definition A distal arthrogryposis characterized by inability to open the mouth fully and pseudocamptodactyly that has_material_basis_in heterozygous mutation in the MYH8 gene on chromosome 17p13.1.
Also Known As "DA7" ; "Dutch-Kentucky syndrome" ; "Hecht syndrome" (for all, see Synonyms field below)
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
 distal arthrogryposis type 7       1
 for disease ribbon | distal arthrogryposis type 7       1
 model of | distal arthrogryposis type 7       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
muscle tissue disease           |
 |__distal arthrogryposis_______|
                                distal arthrogryposis type 7  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a distal arthrogryposis
autosomal dominant disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "DA7" EXACT OMO:0003012
    "Dutch-Kentucky syndrome" EXACT
    "Hecht syndrome" EXACT
    "Hecht-Beals syndrome" EXACT
    "mouth, inability to completely open, and short finger-flexor tendons" EXACT
    "trismus-pseudocamptodactyly syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:2621
MESH:C535857
MIM:121070
MIM:158300
ORDO:3377