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DO Term : non-syndromic X-linked intellectual disability 103 [DOID:0112020] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by intellectual disability and facial feature anomalies that has_material_basis_in hemizygous mutation in the KLHL15 gene on chromosome Xp22.11.
  • synonyms:
  • OMIM:300982,
  • X-linked mental retardation 103,
  • 300982,
  • MRX103
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Disease

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Ontology

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Ontology Term --> Direct parents





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