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DO Term : non-syndromic X-linked intellectual disability 89 [DOID:0112031] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by severe developmental delay that has_material_basis_in heterozygous mutation in a region on chromosome Xp11.3.
  • synonyms:
  • 300848,
  • X-linked mental retardation 89,
  • OMIM:300848,
  • MRX89
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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