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DO Term : orofaciodigital syndrome XI [DOID:0060381] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An orofaciodigital syndrome that is characterized by blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures, low set ears, skeletal malformations, intellectual deficits, deafness and congenital heart defects.
  • synonyms:
  • ORDO:141000,
  • SNOMEDCT_US_2023_03_01:718681002,
  • OMIM:612913,
  • MESH:C557821,
  • UMLS_CUI:C2752048,
  • 612913
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Disease

Diseases --> Human genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents