FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term PEHO syndrome ID (Ontology) DOID:0080539 (Human Disease)
Definition A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss.
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DO.org
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 Genes
 PEHO syndrome       1
 for disease ribbon | PEHO syndrome       1
 model of | PEHO syndrome       1
Spanning Tree (Parents/Children)
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  central nervous system disease
   |__brain disease
       |__PEHO syndrome  1 rec.
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GARD:4264
MESH:C536317
MIM:260565
ORDO:2836