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DO Term : White-Sutton syndrome [DOID:0070067] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene on chromosome 1q21.3.
  • synonyms:
  • OMIM:616364,
  • MRD37,
  • 616364,
  • autosomal dominant mental retardation 37,
  • WHSUS
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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





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