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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:polyradiculoneuropathy
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Accession:DOID:4308 term browser browse the term
Definition:A peripheral nervous system disease that is characterized by the co-occurance of polyneuropahty and polyradicuopathy and is located in both the spinal nerve roots and the peripheral nerves. (DO)
Synonyms:exact_synonym: peripheral autoimmune demyelinating disease;   polyradiculoneuritides;   polyradiculoneuritis;   polyradiculoneuropathies
 primary_id: MESH:D011129
 xref: EFO:1001116
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
chronic inflammatory demyelinating polyradiculoneuropathy term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CCL28 C-C motif chemokine ligand 28 ISO RGD PMID:19050296 RGD:4890012 NCBI chr 4:66,567,139...66,597,310
Ensembl chr 4:66,566,989...66,597,459 		JBrowse link
G CCL5 C-C motif chemokine ligand 5 ISO mRNA:increased expression:sciatic nerve (mouse) RGD PMID:19050296 RGD:4890012 NCBI chr 9:37,817,409...37,823,852
Ensembl chr 9:37,817,305...37,823,852 		JBrowse link
G MMP9 matrix metallopeptidase 9 ISO protein:increased expression:sural nerve RGD PMID:10408538 RGD:13204856 NCBI chr24:33,274,260...33,281,116
Ensembl chr24:33,274,268...33,281,293 		JBrowse link
Guillain-Barre syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AIRE autoimmune regulator ISO OMIM:139393 MouseDO NCBI chr31:38,139,513...38,149,294
Ensembl chr31:38,139,099...38,149,296 		JBrowse link
G APOA4 apolipoprotein A4 ISO protein:increased expression:cerebrospinal fluid (human) RGD PMID:18343991 RGD:5685658 NCBI chr 5:16,751,588...16,754,215
Ensembl chr 5:16,751,799...16,754,837 		JBrowse link
G CCL2 C-C motif chemokine ligand 2 disease_progression ISO protein:increased expression:plasma (human) RGD PMID:12507779 RGD:8549645 NCBI chr 9:39,008,187...39,009,932 JBrowse link
G CD86 CD86 molecule ISO OMIM:139393 MouseDO NCBI chr33:25,256,267...25,318,855
Ensembl chr33:25,256,267...25,318,087 		JBrowse link
G CTSB cathepsin B ISO protein:increased expression:cerebrospinal fluid RGD PMID:11134381 RGD:5686395 NCBI chr25:26,048,237...26,056,570
Ensembl chr25:26,048,253...26,055,801 		JBrowse link
G GDNF glial cell derived neurotrophic factor ISO RGD PMID:9853108 RGD:6218983 NCBI chr 4:70,966,694...70,991,860
Ensembl chr 4:70,971,432...70,989,714 		JBrowse link
G HCRT hypocretin neuropeptide precursor ISO protein:decreased expression:cerebrospinal fluid RGD PMID:15623725 RGD:1600925 NCBI chr 9:20,729,616...20,732,074
Ensembl chr 9:20,730,779...20,732,028 		JBrowse link
G LOC607874 cystatin-C-like ISO protein:decreased expression:cerebrospinal fluid RGD PMID:11134381 RGD:5686395 NCBI chr23:49,562...53,618 JBrowse link
G PMP22 peripheral myelin protein 22 ISO ClinVar Annotator: match by term: Guillain-Barre syndrome, familial OMIM
ClinVar		 PMID:12402337 PMID:25741868 PMID:26392352 PMID:26467025 PMID:28492532 More... NCBI chr 5:38,806,731...38,839,002
Ensembl chr 5:38,807,826...38,838,971 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15721
    disease of anatomical entity 15367
      nervous system disease 13480
        autoimmune disease of the nervous system 592
          polyradiculoneuropathy 12
            Guillain-Barre syndrome + 9
            Radiculoneuropathy, Fatal Neonatal 0
            chronic inflammatory demyelinating polyradiculoneuropathy 3
Path 2
Term Annotations click to browse term
  disease 15721
    disease of anatomical entity 15367
      Immune & Inflammatory Diseases 5200
        immune system disease 4597
          primary immunodeficiency disease 4003
            autoimmune disease 2043
              autoimmune disease of the nervous system 592
                polyradiculoneuropathy 12
                  Guillain-Barre syndrome + 9
                  Radiculoneuropathy, Fatal Neonatal 0
                  chronic inflammatory demyelinating polyradiculoneuropathy 3
paths to the root