FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked parkinsonism-spasticity syndrome ID (Ontology) DOID:0112105 (Human Disease)
Definition A movement disease characterized by slowly progressive development of parkinsonian features and variably penetrant spasticity that has_material_basis_in hemizygous mutation in the ATP6AP2 gene on chromosome Xp11.4.
Also Known As "X-linked Parkinsonism with spasticity" ; "XPDS"
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 Genes
 X-linked parkinsonism-spasticity syndrome       1
 for disease ribbon | X-linked parkinsonism-spasticity syndrome       1
 model of | X-linked parkinsonism-spasticity syndrome       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
brain disease                   |
 |__movement disease____________|
                                X-linked parkinsonism-spasticity syndrome  1 rec.
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Is a X-linked recessive disease
movement disease
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Synonyms
  • "X-linked Parkinsonism with spasticity" EXACT
    "XPDS" EXACT OMO:0003012
Secondary IDs
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MIM:300911
ORDO:363654