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Details
Link-It Detail - Disease - Median Neuropathy
Debug Stats
  • ### Total Build Time: 32 ms 23.694 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 650 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=5 ms Completed: 5 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 560 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.509 KB
  • CONCEPT_RELATIONSHIPS gt=14 ms Completed: 14 ms rowSize= 7.840 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 10.938 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Median Neuropathy C0751922
Definition (1)
Disease involving the median nerve, from its origin at the BRACHIAL PLEXUS to its termination in the hand. Clinical features include weakness of wrist and finger flexion, forearm pronation, thenar abduction, and loss of sensation over the lateral palm, first three fingers, and radial half of the ring finger. Common sites of injury include the elbow, where the nerve passes through the two heads of the pronator teres muscle (pronator syndrome) and in the carpal tunnel (CARPAL TUNNEL SYNDROME).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Mononeuropathies C0494491
Children (1)
img Carpal Tunnel Syndrome C0007286
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278685img Mononeuropathies C0494491
Relationships (19)

Relation Types:
diso_​to_​anat : 3
diso_​to_​diso : 16


Relationships:
none : 13
isa : 5
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT32img Median Nerve C0025058
DISO_to_DISO26img Nerve Compression Syndromes C0027743
DISO_to_DISO21img Carpal Tunnel Syndrome C0007286
DISO_to_DISO19img Ulnar Neuropathies C0154743
DISO_to_DISO16img Nerve Compression Syndromes C0027743
DISO_to_DISO13img 755-756 HAMARTOMAS C0018552
DISO_to_DISO13img Neoplasm of PNS C0031118
DISO_to_ANAT11img Median Nerve C0025058
DISO_to_DISO11img Carpal Tunnel Syndrome C0007286
DISO_to_ANAT10img Fingers C0016129
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_DISO10img Neoplasm of PNS C0031118
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_DISOisaimg Carpal Tunnel Syndrome C0007286
DISO_to_DISOisaimg Injury median nerve C0161457
DISO_to_DISOisaimg Lesion of median nerve C2939189
DISO_to_DISOpermuted_term_ofimg Median Neuropathy C0751922
DISO_to_DISOisaimg Median nerve compression in forearm C0553761
DISO_to_DISOisaimg Median nerve neuritis C0270905
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanUBE3A7337ubiquitin protein ligase E3A
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanTTR7276transthyretin
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanTSC27249tuberous sclerosis 2
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanTSC17248tuberous sclerosis 1
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanCCL26347chemokine (C-C motif) ligand 2
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanPGR5241progesterone receptor
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanIFNG3458interferon, gamma
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanTNC3371tenascin C
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanGALC2581galactosylceramidase
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanCTSS1520cathepsin S
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanCP1356ceruloplasmin (ferroxidase)
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanB2M567beta-2-microglobulin
INFERRED, Score=800, UMLKSK CUI: C0751922
HumanARSB411arylsulfatase B
INFERRED, Score=800, UMLKSK CUI: C0751922
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751922Median Neuropathy0self