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DO Term : chromosome 17q12 deletion syndrome [DOID:0060404] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A chromosomal deletion syndrome that has_material_basis_in a chromosome 17q12 deletion and that is characterized by renal cystic disease, maturity onset diabetes of the young type 5, cognitive impairment, developmental delay (particularly of speech), autistic traits and autism spectrum disorder.
  • synonyms:
  • 17q12 microdeletion syndrome,
  • ICD10CM:Q93.5,
  • 614527,
  • ORDO:261265,
  • OMIM:614527,
  • GARD:13297
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Ontology Term --> Direct children

Ontology Term --> Direct parents