Version: 8.0.0
Date: Tue Jan 28 2025
ring chromosome 20 syndrome
DOID:0070622
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

ring chromosome 20 syndrome

Definition
A ring chromosome syndrome characterized by recognizable epileptic phenotype with typical EEG pattern, intellectual disability manifesting after seizure onset in otherwise normally developing children, and behavioral changes that has_material_basis_in chromosome 20 fusion into a ring or ring-like structure.
Synonyms
  • r(20) syndrome
  • r20 syndrome
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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      Associated Models

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