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DO Term : autosomal dominant intellectual developmental disorder 10 [DOID:0070040] 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 CACNG2 gene on chromosome 22q12.3.
  • synonyms:
  • autosomal dominant mental retardation 10,
  • OMIM:614256,
  • MRD10,
  • 614256,
  • autosomal dominant non-syndromic intellectual disability 10
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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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