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DO Term : non-syndromic X-linked intellectual disability 100 [DOID:0112040] 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 hemizygous mutation in the KIF4A gene on chromosome Xq13.1.
  • synonyms:
  • OMIM:300923,
  • X-linked mental retardation 100,
  • 300923,
  • MRX100
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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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