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Details
Link-It Detail - Disease - Polyneuropathies
Debug Stats
  • ### Total Build Time: 213 ms 39.995 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 763 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=6 ms Completed: 6 ms rowSize= 570 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 3.157 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.526 KB
  • CONCEPT_RELATIONSHIPS gt=141 ms Completed: 141 ms rowSize= 13.529 KB
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 18.754 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Polyneuropathies C0152025
Polyneuropathy
Definition (1)
Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Peripheral Nervous System Diseases C0031117
Children (7)
img Hereditary Sensory and Motor Neuropathy C0027888
img POEMS Syndrome C0085404
img Tangier Disease C0039292
img Alcoholic Neuropathy C0085677
img Hereditary Sensory and Autonomic Neuropathies C0027889
img Polyradiculoneuropathy C0032587
img Paraneoplastic Polyneuropathy C0270932
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278684img Peripheral Nervous System Diseases C0031117
Relationships (83)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 16
diso_​to_​diso : 52
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 59
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 17
mapped_​to : 4
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO101img Complication Aspects C1171258
DISO_to_DISO79img chemically induced C0007994
DISO_to_DISO73img chemically induced C0007994
DISO_to_DISO58img Complication Aspects C1171258
DISO_to_PHEN42img genetic aspects C0017399
DISO_to_DISO35img Myopathy C0026848
DISO_to_DISO29img Demyelinating Diseases C0011303
DISO_to_DISO27img DEMYELINATING DIS C0011303
DISO_to_DISO27img Diabetic Neuropathies C0011882
DISO_to_DISO25img HIV Infections C0019693
DISO_to_PHYS25img Neural Conduction C0027788
DISO_to_DISO22img Critical Illness C0010340
DISO_to_PHEN22img genetic aspects C0017399
DISO_to_PHYS22img Nerve conduction function C0027788
DISO_to_ANAT20img In Blood C0005768
DISO_to_DISO20img Muscular Diseases C0026848
DISO_to_ANAT17img In Blood C0005768
DISO_to_ANAT17img Peripheral Nerves C0031119
DISO_to_CHEM17img Immunoglobulins, Intravenous C0085297
DISO_to_DISO17img Neuralgia C0027796
DISO_to_DISO16img Paraproteinemias C0030489
DISO_to_DISO15img HIV Infections C0019693
DISO_to_DISO15img Muscle Weakness C0151786
DISO_to_DISO15img Vasculitis C0042384
DISO_to_CHEM14img Immunoglobulins, Intravenous C0085297
Genes (81)

Species:
human : 81
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNIPA1123606non imprinted in Prader-Willi/Angelman syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanFGD4121512FYVE, RhoGEF and PH domain containing 4
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanZFYVE27118813zinc finger, FYVE domain containing 27
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanSBF281846SET binding factor 2
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanPRX57716periaxin
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanGDAP154332ganglioside induced differentiation associated protein 1
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanATL151062atlastin GTPase 1
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanST6GALNAC427090ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanHSPB826353heat shock 22kDa protein 8
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanZFYVE2623503zinc finger, FYVE domain containing 26
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanKIF1B23095kinesin family member 1B
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanPARK711315parkinson protein 7
img GENERIF, Score=827, Pubmed Id: 17487420, UMLKSK CUI: C0152025
HumanYWHAQ10971tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta polypeptide
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanSPTLC110558serine palmitoyltransferase, long chain base subunit 1
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanNDRG110397N-myc downstream regulated 1
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanKIF20A10112kinesin family member 20A
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanMFN29927mitofusin 2
img GENERIF, Score=812, Pubmed Id: 17437620, UMLKSK CUI: C0152025
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanLITAF9516lipopolysaccharide-induced TNF factor
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanMTMR28898myotubularin related protein 2
INFERRED, Score=800, UMLKSK CUI: C0152025
HumanCTNNAL18727catenin (cadherin-associated protein), alpha-like 1
INFERRED, Score=800, UMLKSK CUI: C0152025
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0152025Polyneuropathies0self