Search Ontology:
Human Disease

agnathia-otocephaly complex

Term ID
DOID:0060341
Synonyms
  • agnathia-holoprosencephaly-situs inversus syndrome
  • dysgnathia complex agnathia-holoprosencephaly
  • holoprosencephaly-agnathia
  • otocephaly
Definition
A physical disorder characterized by mandibular hypoplasia or agnathia, ventromedial auricular malposition (melotia) and/or auricular fusion (synotia), and microstomia with oroglossal hypoplasia or aglossia. Holoprosencephaly is the most commonly identified association, but skeletal, genitourinary and cardiovascular anomalies and situs inversus have been reported. https://www.ncbi.nlm.nih.gov/pubmed/17438667
References
Ontology
Human Disease   ( DOID:0060341 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.