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DO Term : non-syndromic X-linked intellectual disability 107 [DOID:0112054] 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 heterozygous or hemizygous mutation in CXorf56 on chromosome Xq24.
  • synonyms:
  • OMIM:301013,
  • 301013,
  • X-linked mental retardation 107,
  • MRX107
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents