FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term chromosome 15q24 deletion syndrome ID (Ontology) DOID:0060395 (Human Disease)
Definition A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15.
Also Known As "15q24 microdeletion syndrome"
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 Genes
 chromosome 15q24 deletion syndrome       1
 for disease ribbon | chromosome 15q24 deletion syndrome       1
 model of | chromosome 15q24 deletion syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
chromosomal disease                |
 |__chromosomal deletion syndrome__|
                                   chromosome 15q24 deletion syndrome  1 rec.
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Is a autosomal dominant disease
chromosomal deletion syndrome
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Synonyms
  • "15q24 microdeletion syndrome" EXACT
Secondary IDs
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GARD:12219
ICD10CM:Q93.5
MESH:C579849
MIM:613406
ORDO:94065