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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:nerve compression syndrome
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Accession:DOID:573 term browser browse the term
Definition:Mechanical compression of nerves or nerve roots from internal or external causes. These may result in a conduction block to nerve impulses (due to MYELIN SHEATH dysfunction) or axonal loss. The nerve and nerve sheath injuries may be caused by ISCHEMIA; INFLAMMATION; or a direct mechanical effect.
Synonyms:exact_synonym: Entrapment Neuropathies;   External Nerve Compression Syndromes;   Internal Nerve Compression Syndromes;   Nerve Entrapment;   Nerve Entrapments;   compression neuropathy;   entrapment neuropathy;   nerve compression syndromes;   peripheral nerve entrapment syndrome
 primary_id: MESH:D009408
 xref: NCI:C27221
For additional species annotation, visit the Alliance of Genome Resources.


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nerve compression syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mag myelin-associated glycoprotein IEP RGD PMID:16764860 RGD:9685296 NCBI chr 1:89,345,325...89,360,905
Ensembl chr 1:89,345,429...89,360,733
JBrowse link
G Uck1 uridine-cytidine kinase 1 IEP mRNA:increased expression:spinal cord ventral horn (rat) RGD PMID:10581173 RGD:634248 NCBI chr 3:11,271,874...11,277,757
Ensembl chr 3:11,271,885...11,277,757
JBrowse link
carpal tunnel syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ttr transthyretin ISO ClinVar Annotator: match by term: Carpal tunnel syndrome
ClinVar Annotator: match by term: AMYOTROPHY, THENAR, OF CARPAL ORIGIN
ClinVar Annotator: match by term: Carpal tunnel syndrome, familial
OMIM
ClinVar
PMID:192115, PMID:1351039, PMID:1353008, PMID:1358785, PMID:1490495, PMID:1547960, PMID:1570831, PMID:1867256, PMID:1977686, PMID:1992765, PMID:1997217, PMID:2002274, PMID:2046936, PMID:2063870, PMID:2237288, PMID:2320592, PMID:2349941, PMID:2564060, PMID:2590199, PMID:2624269, PMID:2646319, PMID:2714785, PMID:2856994, PMID:2857043, PMID:2896079, PMID:3011930, PMID:3022107, PMID:3022108, PMID:3022697, PMID:3030336, PMID:3229002, PMID:3457802, PMID:3479441, PMID:3627183, PMID:3908483, PMID:3934968, PMID:4079954, PMID:4138132, PMID:4354899, PMID:5507249, PMID:5652991, PMID:5799493, PMID:6087811, PMID:6100724, PMID:6208668, PMID:6311926, PMID:6549130, PMID:6583672, PMID:6651852, PMID:6736244, PMID:6782125, PMID:7389759, PMID:7839813, PMID:7868124, PMID:8064809, PMID:8100581, PMID:8194279, PMID:8309582, PMID:8563114, PMID:8698351, PMID:8721565, PMID:8778271, PMID:8857732, PMID:9017939, PMID:9215058, PMID:9475090, PMID:10453736, PMID:10465115, PMID:10488818, PMID:10506096, PMID:10529370, PMID:10762172, PMID:10842715, PMID:11385707, PMID:11709003, PMID:11752419, PMID:11752443, PMID:11940682, PMID:12050338, PMID:12217248, PMID:12433265, PMID:12566023, PMID:12617705, PMID:12874413, PMID:12874414, PMID:14569203, PMID:14640030, PMID:14673473, PMID:14986482, PMID:15123043, PMID:15185492, PMID:15249622, PMID:15299606, PMID:15523922, PMID:15820680, PMID:15930086, PMID:16011990, PMID:16194874, PMID:16194875, PMID:16432141, PMID:16631014, PMID:16631015, PMID:17251346, PMID:17503405, PMID:17698792, PMID:18276611, PMID:18318779, PMID:18460047, PMID:18606975, PMID:18830126, PMID:18863976, PMID:18925456, PMID:19364362, PMID:19602727, PMID:19709674, PMID:19781421, PMID:19808383, PMID:20209591, PMID:20301373, PMID:20435197, PMID:21600538, PMID:22083004, PMID:22184092, PMID:22382560, PMID:22531659, PMID:22592564, PMID:22620962, PMID:22745357, PMID:22877808, PMID:22995991, PMID:23080516, PMID:23279339, PMID:23387326, PMID:23414091, PMID:23713495, PMID:23716704, PMID:23833285, PMID:23993291, PMID:24046394, PMID:24073013, PMID:24164154, PMID:24184229, PMID:24455802, PMID:24474780, PMID:24517438, PMID:24555660, PMID:24601850, PMID:24633258, PMID:24800914, PMID:24818650, PMID:24945718, PMID:25225131, PMID:25395306, PMID:25550818, PMID:25551524, PMID:25741868, PMID:25819286, PMID:25846356, PMID:26115788, PMID:26123279, PMID:26428663, PMID:26467025, PMID:26537620, PMID:27793437, PMID:28492532, PMID:28635949, PMID:29121657 NCBI chr18:15,532,963...15,542,180
Ensembl chr18:15,532,963...15,540,177
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16108
    syndrome 6992
      nerve compression syndrome 3
        Meralgia Paraesthetica, Familial 0
        Meralgia Paresthetica 0
        Piriformis Muscle Syndrome + 0
        Pudendal Neuralgia 0
        Superior Transverse Scapular Ligament, Calcification Of, Familial 0
        Ulnar Nerve Compression Syndromes + 0
        carpal tunnel syndrome 1
        tarsal tunnel syndrome 0
        thoracic outlet syndrome + 0
Path 2
Term Annotations click to browse term
  disease 16108
    disease of anatomical entity 15356
      nervous system disease 10865
        peripheral nervous system disease 2472
          nerve compression syndrome 3
            Meralgia Paraesthetica, Familial 0
            Meralgia Paresthetica 0
            Piriformis Muscle Syndrome + 0
            Pudendal Neuralgia 0
            Superior Transverse Scapular Ligament, Calcification Of, Familial 0
            Ulnar Nerve Compression Syndromes + 0
            carpal tunnel syndrome 1
            tarsal tunnel syndrome 0
            thoracic outlet syndrome + 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.