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DO Term : non-syndromic X-linked intellectual disability 19 [DOID:0112019] 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 or heterozygous mutation in the RPS6KA3 gene on chromosome Xp22.12.
  • synonyms:
  • X-linked mental retardation 19,
  • 300844,
  • MRX19,
  • OMIM:300844
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

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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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