Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   neuritis
  

Disease ID 1359
Disease neuritis
Definition
A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA.
Synonym
neuritides
neuritides, peripheral
neuritis (disorder)
neuritis -retired-
neuritis [disease/finding]
neuritis peripheral
neuritis unspecified
neuritis unspecified (disorder)
neuritis, nos
neuritis, peripheral
peripheral neuritides
peripheral neuritis
peripheral neuritis (disorder)
peripheral neuritis, nos
DOID
UMLS
C0027813
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:98)
C0026769  |  multiple sclerosis  |  34
C0027873  |  neuromyelitis optica  |  9
C0011303  |  demyelinating disease  |  6
C0456909  |  blindness  |  4
C0014070  |  encephalomyelitis  |  3
C0019158  |  hepatitis  |  3
C0023343  |  leprosy  |  3
C0392662  |  angiostrongyliasis  |  3
C0019360  |  zoster  |  3
C0024141  |  systemic lupus erythematosus  |  3
C0019360  |  herpes zoster  |  3
C0021053  |  immune disease  |  2
C0034362  |  q fever  |  2
C0019163  |  hepatitis b  |  2
C0271051  |  macular edema  |  2
C0021400  |  influenza  |  2
C0029124  |  optic atrophy  |  2
C0028738  |  nystagmus  |  2
C0011303  |  demyelinating diseases  |  2
C0036454  |  visual field defect  |  2
C0019364  |  herpes zoster ophthalmicus  |  2
C0026975  |  myelitis  |  2
C0442874  |  neuropathy  |  2
C1527336  |  sjogren's syndrome  |  2
C0547030  |  visual disturbance  |  2
C0042164  |  uveitis  |  2
C0042384  |  vasculitis  |  1
C0004943  |  behcet's disease  |  1
C0007959  |  charcot-marie-tooth disease  |  1
C0002736  |  amyotrophic lateral sclerosis  |  1
C0524851  |  neurodegenerative diseases  |  1
C0013990  |  emphysema  |  1
C0003864  |  arthritis  |  1
C0038522  |  subacute sclerosing panencephalitis (sspe)  |  1
C0026764  |  myeloma  |  1
C0020450  |  hyperemesis gravidarum  |  1
C0553662  |  juvenile idiopathic arthritis  |  1
C0015464  |  facial palsy  |  1
C0024419  |  macroglobulinemia  |  1
C0019360  |  herpes zoster infection  |  1
C0032285  |  pneumoniae  |  1
C0008049  |  chicken pox  |  1
C0028754  |  obesity  |  1
C0024419  |  waldenstrom macroglobulinemia  |  1
C0036472  |  scrub typhus  |  1
C0037928  |  myelopathy  |  1
C0014059  |  acute disseminated encephalomyelitis  |  1
C0042721  |  viral hepatitis  |  1
C1692886  |  pyogenic arthritis  |  1
C0155502  |  benign paroxysmal positional vertigo  |  1
C0025297  |  viral meningitis  |  1
C0270911  |  charcot-marie-tooth disease type 1a  |  1
C1834580  |  ramsay hunt syndrome  |  1
C0004943  |  behcet's syndrome  |  1
C0008049  |  chickenpox  |  1
C0011303  |  demyelinating disorders  |  1
C0026896  |  myasthenia gravis  |  1
C0042373  |  vascular disorder  |  1
C0009782  |  connective tissue disorder  |  1
C0030353  |  papilloedema  |  1
C0456909  |  vision loss  |  1
C0023351  |  tuberculoid leprosy  |  1
C0040128  |  thyroid disease  |  1
C0007570  |  celiac disease  |  1
C0020514  |  hyperprolactinaemia  |  1
C0042165  |  anterior uveitis  |  1
C0024198  |  borrelia burgdorferi infection  |  1
C0010346  |  crohn disease  |  1
C0206178  |  cytomegalovirus retinitis  |  1
C0004134  |  ataxia  |  1
C0026764  |  multiple myeloma  |  1
C0014038  |  encephalitis  |  1
C0039128  |  syphilis  |  1
C0524851  |  neurodegenerative disease  |  1
C0042373  |  vascular disorders  |  1
C0598589  |  hereditary neuropathy  |  1
C0235660  |  galactorrhea  |  1
C0036454  |  visual field defects  |  1
C0220754  |  biotinidase deficiency  |  1
C0019364  |  zoster ophthalmicus  |  1
C0243010  |  viral encephalitis  |  1
C0035333  |  retinitis  |  1
C0033953  |  sexual dysfunction  |  1
C0025289  |  meningitis  |  1
C0547030  |  visual disturbances  |  1
C0005122  |  beriberi  |  1
C0043092  |  wegener's granulomatosis  |  1
C0409974  |  lupus erythematosus  |  1
C0041296  |  tuberculosis  |  1
C0235250  |  hyperemesis  |  1
C0042769  |  virus infection  |  1
C0334121  |  inflammatory pseudotumor  |  1
C0014544  |  epilepsy  |  1
C0010346  |  crohn's disease  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0015397  |  ocular disease  |  1
C0038358  |  gastric ulcer  |  1
C0025309  |  meningoencephalitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:148)
6376  |  CX3CL1  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
4804  |  NGFR  |  DISEASES
9423  |  NTN1  |  DISEASES
1723  |  DHODH  |  DISEASES
7040  |  TGFB1  |  DISEASES
5949  |  RBP3  |  DISEASES
6348  |  CCL3  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
3558  |  IL2  |  DISEASES
3458  |  IFNG  |  DISEASES
3820  |  KLRB1  |  DISEASES
3565  |  IL4  |  DISEASES
5657  |  PRTN3  |  DISEASES
6402  |  SELL  |  DISEASES
84918  |  LRP11  |  DISEASES
23435  |  TARDBP  |  DISEASES
10804  |  GJB6  |  DISEASES
27019  |  DNAI1  |  DISEASES
84329  |  HVCN1  |  DISEASES
9098  |  USP6  |  DISEASES
968  |  CD68  |  DISEASES
6351  |  CCL4  |  DISEASES
3630  |  INS  |  DISEASES
348  |  APOE  |  DISEASES
4298  |  MLLT1  |  DISEASES
2056  |  EPO  |  DISEASES
314  |  AOC2  |  DISEASES
6737  |  TRIM21  |  DISEASES
123811  |  FOPNL  |  DISEASES
5375  |  PMP2  |  DISEASES
53  |  ACP2  |  DISEASES
3569  |  IL6  |  DISEASES
7097  |  TLR2  |  DISEASES
109  |  ADCY3  |  DISEASES
6741  |  SSB  |  DISEASES
9172  |  MYOM2  |  DISEASES
8731  |  RNMT  |  DISEASES
3553  |  IL1B  |  DISEASES
23095  |  KIF1B  |  DISEASES
1371  |  CPOX  |  DISEASES
3383  |  ICAM1  |  DISEASES
388  |  RHOB  |  DISEASES
4851  |  NOTCH1  |  DISEASES
9638  |  FEZ1  |  DISEASES
3606  |  IL18  |  DISEASES
7292  |  TNFSF4  |  DISEASES
57105  |  CYSLTR2  |  DISEASES
351  |  APP  |  DISEASES
56896  |  DPYSL5  |  DISEASES
6285  |  S100B  |  DISEASES
729230  |  CCR2  |  DISEASES
1234  |  CCR5  |  DISEASES
92304  |  SCGB3A1  |  DISEASES
6352  |  CCL5  |  DISEASES
7412  |  VCAM1  |  DISEASES
213  |  ALB  |  DISEASES
94234  |  FOXQ1  |  DISEASES
2020  |  EN2  |  DISEASES
4714  |  NDUFB8  |  DISEASES
94274  |  PPP1R14A  |  DISEASES
1632  |  ECI1  |  DISEASES
3627  |  CXCL10  |  DISEASES
64446  |  DNAI2  |  DISEASES
344561  |  GPR148  |  DISEASES
5376  |  PMP22  |  DISEASES
8534  |  CHST1  |  DISEASES
4744  |  NEFH  |  DISEASES
5551  |  PRF1  |  DISEASES
80381  |  CD276  |  DISEASES
491  |  ATP2B2  |  DISEASES
9033  |  PKD2L1  |  DISEASES
55748  |  CNDP2  |  DISEASES
2187  |  FANCB  |  DISEASES
1668  |  DEFA3  |  DISEASES
83733  |  SLC25A18  |  DISEASES
64782  |  AEN  |  DISEASES
942  |  CD86  |  DISEASES
90249  |  UNC5A  |  DISEASES
5133  |  PDCD1  |  DISEASES
342035  |  GLDN  |  DISEASES
5025  |  P2RX4  |  DISEASES
3363  |  HTR7  |  DISEASES
6622  |  SNCA  |  DISEASES
59277  |  NTN4  |  DISEASES
921  |  CD5  |  DISEASES
3605  |  IL17A  |  DISEASES
23114  |  NFASC  |  DISEASES
9600  |  PITPNM1  |  DISEASES
3177  |  SLC29A2  |  DISEASES
1524  |  CX3CR1  |  DISEASES
4133  |  MAP2  |  DISEASES
54106  |  TLR9  |  DISEASES
9846  |  GAB2  |  DISEASES
4538  |  MT-ND4  |  DISEASES
5743  |  PTGS2  |  DISEASES
962  |  CD48  |  DISEASES
115352  |  FCRL3  |  DISEASES
914  |  CD2  |  DISEASES
4803  |  NGF  |  DISEASES
282991  |  BLOC1S2  |  DISEASES
2334  |  AFF2  |  DISEASES
959  |  CD40LG  |  DISEASES
680  |  BRS3  |  DISEASES
958  |  CD40  |  DISEASES
4318  |  MMP9  |  DISEASES
9469  |  CHST3  |  DISEASES
10800  |  CYSLTR1  |  DISEASES
6191  |  RPS4X  |  DISEASES
2833  |  CXCR3  |  DISEASES
1896  |  EDA  |  DISEASES
3339  |  HSPG2  |  DISEASES
54829  |  ASPN  |  DISEASES
6392  |  SDHD  |  DISEASES
199  |  AIF1  |  DISEASES
50943  |  FOXP3  |  DISEASES
1041  |  CDSN  |  DISEASES
7454  |  WAS  |  DISEASES
4340  |  MOG  |  DISEASES
9445  |  ITM2B  |  DISEASES
4897  |  NRCAM  |  DISEASES
646480  |  FABP9  |  DISEASES
7293  |  TNFRSF4  |  DISEASES
22866  |  CNKSR2  |  DISEASES
3456  |  IFNB1  |  DISEASES
3662  |  IRF4  |  DISEASES
4155  |  MBP  |  DISEASES
361  |  AQP4  |  DISEASES
4099  |  MAG  |  DISEASES
9244  |  CRLF1  |  DISEASES
2596  |  GAP43  |  DISEASES
374654  |  KIF7  |  DISEASES
64400  |  AKTIP  |  DISEASES
6164  |  RPL34  |  DISEASES
9255  |  AIMP1  |  DISEASES
4905  |  NSF  |  DISEASES
25983  |  NGDN  |  DISEASES
7124  |  TNF  |  DISEASES
4049  |  LTA  |  DISEASES
4152  |  MBD1  |  DISEASES
388372  |  CCL4L1  |  DISEASES
81704  |  DOCK8  |  DISEASES
2668  |  GDNF  |  DISEASES
3586  |  IL10  |  DISEASES
627  |  BDNF  |  DISEASES
4359  |  MPZ  |  DISEASES
54970  |  TTC12  |  DISEASES
Locus(Waiting for update.)
Disease ID 1359
Disease neuritis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:57)
HP:0000572  |  Visual loss  |  8
HP:0011096  |  Demyelination  |  5
HP:0000618  |  Blindness  |  4
HP:0040078  |  Axonal degeneration  |  3
HP:0001945  |  Fever  |  3
HP:0012115  |  Liver inflammation  |  3
HP:0002725  |  Systemic lupus erythematosus  |  3
HP:0000639  |  Nystagmus  |  2
HP:0012531  |  Pain  |  2
HP:0012486  |  Inflammation of spinal cord  |  2
HP:0040049  |  Macular edema  |  2
HP:0002321  |  Vertigo  |  2
HP:0100829  |  Galactorrhoea  |  2
HP:0000505  |  Poor vision  |  2
HP:0002180  |  Neurodegeneration  |  2
HP:0000648  |  Optic-nerve degeneration  |  2
HP:0002960  |  Autoimmune condition  |  2
HP:0001123  |  Partial loss of field of vision  |  2
HP:0000554  |  Uveitis  |  2
HP:0030528  |  Paracentral scotoma  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0001287  |  Meningitis  |  1
HP:0005318  |  Cerebral vasculitis  |  1
HP:0001251  |  Ataxia  |  1
HP:0005508  |  Waldenstrom macroglobulinemia  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0002664  |  Neoplasia  |  1
HP:0000016  |  Urinary retention  |  1
HP:0002383  |  Encephalitis  |  1
HP:0001513  |  Obesity  |  1
HP:0006562  |  Viral hepatitis  |  1
HP:0000870  |  Hyperprolactinemia  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0007354  |  Amyotrophic lateral sclerosis  |  1
HP:0002597  |  Abnormality of blood vessels  |  1
HP:0000529  |  Slowly progressive visual loss  |  1
HP:0003447  |  Axonal loss  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0100561  |  Spinal cord lesion  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0010628  |  Facial palsy, unilateral or bilateral  |  1
HP:0007663  |  Central visual loss  |  1
HP:0002097  |  Pulmonary emphysema  |  1
HP:0012122  |  Anterior uveitis  |  1
HP:0002592  |  Stomach ulcer  |  1
HP:0001369  |  Arthritis  |  1
HP:0001171  |  Hand ectrodactyly  |  1
HP:0002608  |  Celiac disease  |  1
HP:0012188  |  Hyperemesis gravidarum  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0005681  |  Juvenile idiopathic arthritis  |  1
HP:0002196  |  Myelopathy  |  1
HP:0002883  |  Rapid breathing  |  1
HP:0000969  |  Dropsy  |  1
HP:0100246  |  Osteoma  |  1
HP:0002633  |  Vasculitis  |  1
HP:0000603  |  Central scotomata  |  1
Disease ID 1359
Disease neuritis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0030193  |  pain  |  2
C0030353  |  papilloedema  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:9)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0027813fluorouracilD00547251-21-8neuritisMESH:D009443marker/mechanism17430663
C0027813leucovorinD0029551958/5/9neuritisMESH:D009443marker/mechanism17430663
C0027813foscarnetD0172454428-95-9neuritisMESH:D009443marker/mechanism9761526
C0027813lidocaineD008012137-58-6neuritisMESH:D009443marker/mechanism19224819
C0027813oxaliplatinC030110-neuritisMESH:D009443marker/mechanism17430663
C0027813paclitaxelD017239-neuritisMESH:D009443marker/mechanism8893892
C0027813thalidomideD01379250-35-1neuritisMESH:D009443marker/mechanism7579470
C0027813vinblastineD014747865-21-4neuritisMESH:D009443marker/mechanism5768441
C0027813vinorelbineC03085271486-22-1neuritisMESH:D009443marker/mechanism18819904
FDA approved drug and dosage information(Total Drugs:3)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D009443eloxatinoxaliplatin50MG/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsINJECTABLE;IV (INFUSION)DiscontinuedNoneYesNo
MESH:D009443eloxatinoxaliplatin50MG/10ML (5MG/ML)INJECTABLE;IV (INFUSION)PrescriptionAPYesYes
MESH:D009443oxaliplatinoxaliplatin50MG/10ML (5MG/ML)INJECTABLE;IV (INFUSION)PrescriptionAPYesYes
FDA labeling changes(Total Drugs:3)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D00944310/1/2007eloxatinoxaliplatinSolid tumorsThe effectiveness of oxaliplatin in children has not been established No significant activity observed in 2 Phase I and 2 Phase II trials in 159 patients ages 7 months to 22 years with solid tumors Information on clinical studies and AEsLabelingB---Sanofi-Aventis09/27/2006FALSE'
MESH:D00944310/1/2007eloxatinoxaliplatinSolid tumorsThe effectiveness of oxaliplatin in children has not been established No significant activity observed in 2 Phase I and 2 Phase II trials in 159 patients ages 7 months to 22 years with solid tumors Information on clinical studies and AEsLabelingB---Sanofi-Aventis09/27/2006FALSE'
MESH:D00944310/1/2007eloxatinoxaliplatinSolid tumorsThe effectiveness of oxaliplatin in children has not been established No significant activity observed in 2 Phase I and 2 Phase II trials in 159 patients ages 7 months to 22 years with solid tumors Information on clinical studies and AEsLabelingB---Sanofi-Aventis09/27/2006FALSE'