ONTOLOGY REPORT - ANNOTATIONS


Term:facial paralysis
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Accession:DOID:13934 term browser browse the term
Definition:Severe or complete loss of facial muscle motor function. This condition may result from central or peripheral lesions. Damage to CNS motor pathways from the cerebral cortex to the facial nuclei in the pons leads to facial weakness that generally spares the forehead muscles. FACIAL NERVE DISEASES generally results in generalized hemifacial weakness. NEUROMUSCULAR JUNCTION DISEASES and MUSCULAR DISEASES may also cause facial paralysis or paresis.
Synonyms:exact_synonym: Central Facial Paralysis;   Facial Palsies;   Facial Palsy;   Facial Paralyses, Peripheral;   Facial Paresis;   Hemifacial Paralysis;   Lower Motor Neuron Facial Palsy;   Paralyses, Facial;   Paralyses, Hemifacial;   Pareses, Facial;   Peripheral Facial Paralysis;   central facial paralyses;   upper motor neuron facial palsy
 primary_id: MESH:D005158
 alt_id: RDO:0000420
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facial paralysis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mmp9 matrix metallopeptidase 9 JBrowse link 3 161,413,410 161,421,473 RGD:8547852
G Pomc proopiomelanocortin JBrowse link 6 28,382,937 28,388,771 RGD:11554173
Cayler Cardiofacial Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Eya1 EYA transcriptional coactivator and phosphatase 1 JBrowse link 5 4,275,728 4,495,525 RGD:11554173
FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tubb6 tubulin, beta 6 class V JBrowse link 18 63,130,542 63,140,181 RGD:8554872
RGD:7240710
Hereditary Congenital Facial Paresis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hoxb1 homeo box B1 JBrowse link 10 84,214,358 84,215,812 RGD:11554173
Hereditary Congenital Facial Paresis 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hoxb1 homeo box B1 JBrowse link 10 84,214,358 84,215,812 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    sensory system disease 4246
      mouth disease 660
        facial nerve disease 49
          facial paralysis 5
            Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma 0
            Bell's palsy 0
            Cayler Cardiofacial Syndrome 1
            Congenital Facial Palsy, Unilateral or Bilateral 0
            FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION 1
            Facial Palsy, Familial Recurrent Peripheral 0
            Foix Chavany Marie Syndrome 0
            Hereditary Congenital Facial Paresis + 1
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        peripheral nervous system disease 2009
          neuropathy 1830
            cranial nerve disease 356
              facial nerve disease 49
                facial paralysis 5
                  Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma 0
                  Bell's palsy 0
                  Cayler Cardiofacial Syndrome 1
                  Congenital Facial Palsy, Unilateral or Bilateral 0
                  FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION 1
                  Facial Palsy, Familial Recurrent Peripheral 0
                  Foix Chavany Marie Syndrome 0
                  Hereditary Congenital Facial Paresis + 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.