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DO Term : Joubert syndrome [DOID:0050777] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones.
  • synonyms:
  • GARD:6802,
  • OMIM:PS213300,
  • ORDO:475,
  • JBTS,
  • PS213300,
  • ICD10CM:Q04.3
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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