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DO Term : Clark-Baraitser syndrome [DOID:0080234] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.
  • synonyms:
  • autosomal dominant mental retardation 49,
  • MESH:C536208,
  • Baraitser syndrome,
  • OMIM:617752,
  • GARD:13584,
  • 617752,
  • CLABARS,
  • autosomal dominant intellectual disability 49
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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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