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DO Term : autosomal dominant intellectual developmental disorder 21 [DOID:0070051] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTCF gene on chromosome 16q22.1.
  • synonyms:
  • 615502,
  • autosomal dominant mental retardation 21,
  • autosomal dominant non-syndromic intellectual disability 21,
  • OMIM:615502,
  • MRD21
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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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