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DO Term : non-syndromic X-linked intellectual disability ARX-related [DOID:0112021] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by moderate to profound intellectual disability with variable additional features that has_material_basis_in hemizygous mutation in ARX on chromosome Xp21.3.
  • synonyms:
  • X-linked mental retardation 54,
  • X-linked mental retardation 52,
  • 300419,
  • X-linked mental retardation with or without seizures ARX-related,
  • X-linked mental retardation 76,
  • X-linked mental retardation 32,
  • GARD:5614,
  • X-linked mental retardation 87,
  • OMIM:300419,
  • X-linked mental retardation 29,
  • ARX-related intellectual disability,
  • X-linked mental retardation 38,
  • X-linked mental retardation 33,
  • X-linked mental retardation 29 and others,
  • MRXARX,
  • X-linked mental retardation 43
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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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