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DO Term : non-syndromic X-linked intellectual disability 41 [DOID:0112058] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in heterozygous mutation in the GDI1 gene on chromosome Xq28.
  • synonyms:
  • X-linked mental retardation 41,
  • MRX48,
  • MRX41,
  • OMIM:300849,
  • 300849,
  • X-linked mental retardation 48
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Ontology

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Ontology Term --> Direct parents