FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cerebral palsy ID (Ontology) DOID:1969 (Human Disease)
Definition A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance.
Also Known As "infantile cerebral palsy"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       3
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 cerebral palsy       3      1
 model of | cerebral palsy       3       --
Spanning Tree (Parents/Children)
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  central nervous system disease
   |__brain disease
       |__cerebral palsy  13 rec.
           |__ataxic cerebral palsy
           |__dyskinetic cerebral palsy
           |__mixed cerebral palsy
           |__spastic cerebral palsy 10 rec.
               |__spastic diplegia
               |__spastic hemiplegia
               |__spastic monoplegia
               |__spastic quadriplegic cerebral palsy(+) 10 rec.
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Is a brain disease
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Synonyms
  • "infantile cerebral palsy" EXACT
Secondary IDs
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ICD10CM:G80
MESH:D002547
NCI:C34460
SNOMEDCT_US_2023_03_01:155024003
UMLS_CUI:C0007789