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Details
Link-It Detail - Disease - Paresthesia
Debug Stats
  • ### Total Build Time: 50 ms 31.199 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 320 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 368 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=0 Completed: 0 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.815 KB
  • CONCEPT_RELATIONSHIPS gt=27 ms Completed: 27 ms rowSize= 12.793 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 13.013 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Paresthesia C0030554
Definition (1)
A disorder characterized by functional disturbances of sensory neurons resulting in abnormal cutaneous sensations of tingling, numbness, pressure, cold, and warmth that are experienced in the absence of a stimulus.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Somatosensory Disorders C0752262
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Somatosensory Disorders C0752262
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Somatosensory Disorders C0752262
Relationships (75)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 9
diso_​to_​diso : 53
diso_​to_​phys : 2


Relationships:
none : 51
disease_​may_​have_​finding : 1
isa : 8
mapped_​to : 14
replaces : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO58img chemically induced C0007994
DISO_to_DISO50img chemically induced C0007994
DISO_to_DISO20img Nerve Compression Syndromes C0027743
DISO_to_DISO16img COMPL POSTOP C0032787
DISO_to_DISO15img Nerve Compression Syndromes C0027743
DISO_to_ANAT14img Mandibular Nerve C0024695
DISO_to_DISO14img Pain C0030193
DISO_to_ANAT13img Hand C0018563
DISO_to_CHEM13img Anesthetics, Local C0002934
DISO_to_DISO12img Erythema C0041834
DISO_to_DISO12img FEMORAL NERVE DIS C0751931
DISO_to_DISO12img Hypesthesia C0020580
DISO_to_DISO12img Muscle Weakness C0151786
DISO_to_CHEM11img Anesthetics, Local C0002934
DISO_to_DISO11img Carpal Tunnel Syndrome C0007286
DISO_to_DISO11img Pain C0030193
DISO_to_CHEM10img Antineoplastic Agents C0003392
DISO_to_DISO10img COMPL POSTOP C0032787
DISO_to_DISO10img Cranial Nerve V Injury C0161406
DISO_to_DISO10img Dermatoses, Hand C0018567
DISO_to_ANAT9img Hand C0018563
DISO_to_ANAT9img Mandibular Nerve C0024695
DISO_to_CHEM9img Articaine C1608295
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_DISO9img Dermatoses, Foot C0016509
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanCD24100133941CD24 molecule
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanAMN81693amnion associated transmembrane protein
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanMTHFR4524methylenetetrahydrofolate reductase (NAD(P)H)
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanCIITA4261class II, major histocompatibility complex, transactivator
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanIL7R3575interleukin 7 receptor
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanHMBS3145hydroxymethylbilane synthase
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanHLA-DRB13123
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanGIF2694gastric intrinsic factor (vitamin B synthesis)
img OMIM, Score=1000, UMLKSK CUI: C0030554
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img OMIM, Score=1000, UMLKSK CUI: C0030554
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030554Paresthesia0self