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DO Term : non-syndromic X-linked intellectual disability 58 [DOID:0112024] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability and no consistent dysmorphic features that has_material_basis_in hemizygous mutation in the TSPAN7 gene on chromosome Xp11.4.
  • synonyms:
  • OMIM:300210,
  • MRX58,
  • 300210,
  • X-linked mental retardation 58
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Disease

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Ontology

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Ontology Term --> Direct parents





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