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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:Bell's palsy
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Accession:DOID:12506 term browser browse the term
Definition:A facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve). (DO)
Synonyms:exact_synonym: Acute Inflammatory Facial Neuropathy;   Bell palsies;   Bell palsy;   Bell's (facial) palsy;   Bell's Palsies;   Bells Palsy;   Herpetic Facial Paralyses;   Herpetic Facial Paralysis;   acute idiopathic facial neuropathy;   idiopathic facial paralyses;   idiopathic facial paralysis
 primary_id: MESH:D020330
 xref: EFO:0007167;   GARD:5906;   ICD9CM:351.0
For additional species annotation, visit the Alliance of Genome Resources.

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Bell's palsy term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ppia peptidylprolyl isomerase A exacerbates ISO protein:increased expression:blood serum (human) RGD PMID:32149981 RGD:150429625 NCBI chr14:81,279,292...81,282,960
Ensembl chr14:81,275,091...81,299,601
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21086
    syndrome 10782
      Bell's palsy 1
Path 2
Term Annotations click to browse term
  disease 21086
    disease of anatomical entity 18146
      nervous system disease 13993
        Neurologic Manifestations 9942
          sensory system disease 6847
            mouth disease 935
              facial nerve disease 53
                facial paralysis 6
                  Bell's palsy 1
paths to the root