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DO Term : biotin-responsive basal ganglia disease [DOID:0050659] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A basal ganglia disease that is characterized by recurrent subacute encephalopathy, has_symptom confusion, has_symptom seizure, has_symptom ataxia, has_symptom dystonia, has_symptom supranuclear facial palsy, has_symptom external ophthalmoplegia, and has_symptom dysphagia.
  • synonyms:
  • 607483,
  • MESH:C537658,
  • OMIM:607483
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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