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DO Term : non-syndromic X-linked intellectual disability 42 [DOID:0112057] 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 mutation in a region on chromosome Xq26.
  • synonyms:
  • OMIM:300372,
  • MRX42,
  • X-linked mental retardation 42,
  • 300372
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Disease

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Ontology

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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