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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:pseudobulbar palsy
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Accession:DOID:12680 term browser browse the term
Definition:A brain disease that is characterized by damage to neurons of the corticobulbar tract, has_symptom dysarthria, has_symptom dysphagia, has_symptom spasticity located_in tongue, has_symptom gag reflex, and has_symptom emotional outbursts. (DO)
Synonyms:exact_synonym: Pseudobulbar Dysarthria;   Pseudobulbar Mutism;   Pseudobulbar Paralysis;   Pseudobulbar Pareses;   pseudobulbar dysarthrias;   pseudobulbar mutisms;   pseudobulbar palsies;   pseudobulbar paresis;   pseudobulbar syndrome;   pseudobulbar syndromes;   spastic bulbar palsies;   spastic bulbar palsy
 primary_id: MESH:D020828
 xref: EFO:1001131;   ICD9CM:335.23;   NCI:C129934
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21089
    syndrome 10784
      pseudobulbar palsy 0
        Kuzniecky Andermann Syndrome 0
Path 2
Term Annotations click to browse term
  disease 21089
    disease of anatomical entity 18156
      nervous system disease 13996
        peripheral nervous system disease 4059
          neuropathy 3838
            neuromuscular disease 3023
              motor neuron disease 521
                pseudobulbar palsy 0
                  Kuzniecky Andermann Syndrome 0
paths to the root