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Details
Link-It Detail - Disease - Nerve Compression Syndromes
Debug Stats
  • ### Total Build Time: 212 ms 30.122 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 451 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 570 bytes
  • CONCEPT_CHILDREN gt=26 ms Completed: 26 ms rowSize= 2.284 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.526 KB
  • CONCEPT_RELATIONSHIPS gt=131 ms Completed: 131 ms rowSize= 12.605 KB
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 10.938 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Nerve Compression Syndromes C0027743
Nerve compression syndrome
Definition (1)
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.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Peripheral Nervous System Diseases C0031117
Children (5)
img Piriformis Muscle Syndrome C0458224
img Tarsal Tunnel Syndrome C0039319
img Ulnar Nerve Compression Syndromes C0206242
img Thoracic Outlet Syndrome C0039984
img Carpal Tunnel Syndrome C0007286
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278684img Peripheral Nervous System Diseases C0031117
Relationships (82)

Relation Types:
diso_​to_​anat : 36
diso_​to_​diso : 45
diso_​to_​phys : 1


Relationships:
none : 80
mapped_​to : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO138img Complication Aspects C1171258
DISO_to_DISO109img Complication Aspects C1171258
DISO_to_ANAT47img Spinal Nerve Roots C0037940
DISO_to_ANAT46img Spinal Nerve Roots C0037940
DISO_to_DISO44img Disorder of the optic nerve C0029132
DISO_to_DISO37img Optic Nerve Diseases C0029132
DISO_to_ANAT36img Muscle, Skeletal C0242692
DISO_to_DISO34img Radial Neuropathy C0748226
DISO_to_DISO31img COMPL POSTOP C0032787
DISO_to_DISO31img Neuralgia C0027796
DISO_to_DISO31img Radial Neuropathy C0748226
DISO_to_DISO30img Trigeminal Neuralgia C0040997
DISO_to_ANAT28img Bone structure of lumbar vertebra C0024091
DISO_to_ANAT27img Muscle, Skeletal C0242692
DISO_to_DISO27img FIBULAR NERVE DIS C0747533
DISO_to_DISO27img Peripheral Nervous System Diseases C0031117
DISO_to_DISO26img Median Neuropathy C0751922
DISO_to_ANAT25img Bone structure of scapula C0036277
DISO_to_DISO25img COMPL POSTOP C0032787
DISO_to_DISO25img Trigeminal Neuralgia C0040997
DISO_to_DISO23img Peripheral Nervous System Diseases C0031117
DISO_to_ANAT22img Cauda Equina C0007458
DISO_to_ANAT22img Structure of radial nerve C0034518
DISO_to_DISO22img NEUROPATHY, SCIATIC C0149940
DISO_to_ANAT21img Joint structure of shoulder region C0037009
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanUBE3A7337ubiquitin protein ligase E3A
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanTTR7276transthyretin
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanTSC27249tuberous sclerosis 2
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanTSC17248tuberous sclerosis 1
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanCCL26347chemokine (C-C motif) ligand 2
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanPGR5241progesterone receptor
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanIFNG3458interferon, gamma
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanTNC3371tenascin C
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanGALC2581galactosylceramidase
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanCTSS1520cathepsin S
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanCP1356ceruloplasmin (ferroxidase)
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanB2M567beta-2-microglobulin
INFERRED, Score=800, UMLKSK CUI: C0027743
HumanARSB411arylsulfatase B
INFERRED, Score=800, UMLKSK CUI: C0027743
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0027743Nerve Compression Syndromes0self