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DO Term : non-syndromic X-linked intellectual disability 73 [DOID:0112017] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability in males that has_material_basis_in hemizygous mutation in a region on chromosome Xp22.2.
  • synonyms:
  • OMIM:300355,
  • X-linked mental retardation 73,
  • 300355,
  • MRX73
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Disease

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Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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