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DO Term : chromosome 8q21.11 deletion syndrome [DOID:0060425] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 8q21.11 region and that is characterized by intellectual disability and common facial dysmorphic features.
  • synonyms:
  • 8q21.11 microdeletion syndrome,
  • ORDO:284160,
  • 614230,
  • OMIM:614230,
  • ICD10CM:Q93.5
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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