FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term spastic paraplegia with deafness ID (Ontology) DOID:0081100 (Human Disease)
Definition A hereditary spastic paraplegia that is characterized spastic paraplegia, tremor, cataracts, deafness, short stature, and hypogonadism presenting in the end of the first decade of life.
Also Known As "Spastic paraparesis-deafness syndrome" ; "Wells Jankovic Syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
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
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
X-linked monogenic disease
 |__X-linked recessive disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   spastic paraplegia with deafness
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a X-linked recessive disease
hereditary spastic paraplegia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Spastic paraparesis-deafness syndrome" EXACT
    "Wells Jankovic Syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:5555
MESH:C536692
MIM:312910
ORDO:2815