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Pediatric Disease Annotations & Medicines



   axonal neuropathy
  

Disease ID 974
Disease axonal neuropathy
Definition
Any nerve disorder affecting the axon of a nerve.
Synonym
axonal neuropathies
axonal neuropathy (disorder)
axonal neuropathy, nos
DOID
UMLS
C0270921
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:31)
C0007758  |  cerebellar ataxia  |  26
C0004134  |  ataxia  |  25
C0030486  |  paraplegia  |  4
C0242287  |  neuromyotonia  |  3
C0152025  |  polyneuropathy  |  2
C0037773  |  hereditary spastic paraplegia  |  2
C0524851  |  neurodegenerative disease  |  2
C0018378  |  guillain-barre syndrome  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0878544  |  cardiomyopathy  |  1
C0026846  |  muscular atrophy  |  1
C0206744  |  idiopathic cd4+ t-lymphocytopenia  |  1
C0175704  |  leopard syndrome  |  1
C0393799  |  fisher syndrome  |  1
C0021400  |  influenza  |  1
C0279637  |  anal carcinoma  |  1
C0021670  |  insulinoma  |  1
C0024312  |  lymphocytopenia  |  1
C0011847  |  diabetes  |  1
C1527336  |  sjogren syndrome  |  1
C0151313  |  sensory neuropathy  |  1
C0016719  |  friedreich ataxia  |  1
C0206744  |  cd4+ t-lymphocytopenia  |  1
C0011849  |  diabetes mellitus  |  1
C1704437  |  respiratory distress syndrome  |  1
C0030567  |  parkinson's disease  |  1
C0393799  |  miller-fisher syndrome  |  1
C0026848  |  myopathy  |  1
C0007194  |  hypertrophic cardiomyopathy  |  1
C0442874  |  neuropathy  |  1
C0037769  |  west syndrome  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:186)
6820  |  SULT2B1  |  DISEASES
51324  |  SPG21  |  DISEASES
6948  |  TCN2  |  DISEASES
9517  |  SPTLC2  |  DISEASES
7443  |  VRK1  |  DISEASES
113278  |  SLC52A3  |  DISEASES
5173  |  PDYN  |  DISEASES
79152  |  FA2H  |  DISEASES
54332  |  GDAP1  |  DISEASES
4849  |  CNOT3  |  DISEASES
23064  |  SETX  |  DISEASES
5193  |  PEX12  |  DISEASES
1337  |  COX6A1  |  DISEASES
4358  |  MPV17  |  DISEASES
9927  |  MFN2  |  DISEASES
7276  |  TTR  |  DISEASES
10342  |  TFG  |  DISEASES
80218  |  NAA50  |  DISEASES
9409  |  PEX16  |  DISEASES
1959  |  EGR2  |  DISEASES
6310  |  ATXN1  |  DISEASES
11034  |  DSTN  |  DISEASES
4974  |  OMG  |  DISEASES
8139  |  GAN  |  DISEASES
3315  |  HSPB1  |  DISEASES
23503  |  ZFYVE26  |  DISEASES
7251  |  TSG101  |  DISEASES
1890  |  TYMP  |  DISEASES
25814  |  ATXN10  |  DISEASES
91574  |  C12orf65  |  DISEASES
55065  |  SLC52A1  |  DISEASES
3508  |  IGHMBP2  |  DISEASES
81846  |  SBF2  |  DISEASES
271  |  AMPD2  |  DISEASES
7274  |  TTPA  |  DISEASES
2581  |  GALC  |  DISEASES
3093  |  UBE2K  |  DISEASES
59341  |  TRPV4  |  DISEASES
16  |  AARS  |  DISEASES
80208  |  SPG11  |  DISEASES
9172  |  MYOM2  |  DISEASES
10558  |  SPTLC1  |  DISEASES
7515  |  XRCC1  |  DISEASES
81930  |  KIF18A  |  DISEASES
8424  |  BBOX1  |  DISEASES
421  |  ARVCF  |  DISEASES
5582  |  PRKCG  |  DISEASES
23095  |  KIF1B  |  DISEASES
57679  |  ALS2  |  DISEASES
27338  |  UBE2S  |  DISEASES
1356  |  CP  |  DISEASES
950  |  SCARB2  |  DISEASES
7879  |  RAB7A  |  DISEASES
4885  |  NPTX2  |  DISEASES
50846  |  DHH  |  DISEASES
5428  |  POLG  |  DISEASES
6687  |  SPG7  |  DISEASES
9515  |  STXBP5L  |  DISEASES
5723  |  PSPH  |  DISEASES
472  |  ATM  |  DISEASES
3145  |  HMBS  |  DISEASES
291  |  SLC25A4  |  DISEASES
26353  |  HSPB8  |  DISEASES
9131  |  AIFM1  |  DISEASES
5192  |  PEX10  |  DISEASES
50852  |  TRAT1  |  DISEASES
10085  |  EDIL3  |  DISEASES
27242  |  TNFRSF21  |  DISEASES
9907  |  AP5Z1  |  DISEASES
90678  |  LRSAM1  |  DISEASES
8988  |  HSPB3  |  DISEASES
5190  |  PEX6  |  DISEASES
3094  |  HINT1  |  DISEASES
84233  |  TMEM126A  |  DISEASES
5376  |  PMP22  |  DISEASES
1808  |  DPYSL2  |  DISEASES
83858  |  ATAD3B  |  DISEASES
4744  |  NEFH  |  DISEASES
6773  |  STAT2  |  DISEASES
1604  |  CD55  |  DISEASES
274  |  BIN1  |  DISEASES
58492  |  ZNF77  |  DISEASES
10397  |  NDRG1  |  DISEASES
547  |  KIF1A  |  DISEASES
11284  |  PNKP  |  DISEASES
3032  |  HADHB  |  DISEASES
57716  |  PRX  |  DISEASES
80821  |  DDHD1  |  DISEASES
23400  |  ATP13A2  |  DISEASES
113612  |  CYP2U1  |  DISEASES
79581  |  SLC52A2  |  DISEASES
55256  |  ADI1  |  DISEASES
342184  |  FMN1  |  DISEASES
342035  |  GLDN  |  DISEASES
91010  |  FMNL3  |  DISEASES
55775  |  TDP1  |  DISEASES
3300  |  DNAJB2  |  DISEASES
23321  |  TRIM2  |  DISEASES
1180  |  CLCN1  |  DISEASES
9516  |  LITAF  |  DISEASES
966  |  CD59  |  DISEASES
9639  |  ARHGEF10  |  DISEASES
5498  |  PPOX  |  DISEASES
875  |  CBS  |  DISEASES
56704  |  JPH1  |  DISEASES
3005  |  H1F0  |  DISEASES
4771  |  NF2  |  DISEASES
23114  |  NFASC  |  DISEASES
8898  |  MTMR2  |  DISEASES
3792  |  KEL  |  DISEASES
1785  |  DNM2  |  DISEASES
91137  |  SLC25A46  |  DISEASES
273  |  AMPH  |  DISEASES
22931  |  RAB18  |  DISEASES
5828  |  PEX2  |  DISEASES
51062  |  ATL1  |  DISEASES
55814  |  BDP1  |  DISEASES
773  |  CACNA1A  |  DISEASES
23230  |  VPS13A  |  DISEASES
25894  |  PLEKHG4  |  DISEASES
26580  |  BSCL2  |  DISEASES
6663  |  SOX10  |  DISEASES
7150  |  TOP1  |  DISEASES
4508  |  MT-ATP6  |  DISEASES
2705  |  GJB1  |  DISEASES
55157  |  DARS2  |  DISEASES
4509  |  MT-ATP8  |  DISEASES
5071  |  PARK2  |  DISEASES
23345  |  SYNE1  |  DISEASES
910  |  CD1B  |  DISEASES
4000  |  LMNA  |  DISEASES
9531  |  BAG3  |  DISEASES
2010  |  EMD  |  DISEASES
959  |  CD40LG  |  DISEASES
10555  |  AGPAT2  |  DISEASES
6834  |  SURF1  |  DISEASES
5476  |  CTSA  |  DISEASES
229  |  ALDOB  |  DISEASES
2395  |  FXN  |  DISEASES
57449  |  PLEKHG5  |  DISEASES
57704  |  GBA2  |  DISEASES
55210  |  ATAD3A  |  DISEASES
219293  |  ATAD3C  |  DISEASES
4897  |  NRCAM  |  DISEASES
54840  |  APTX  |  DISEASES
3030  |  HADHA  |  DISEASES
6606  |  SMN1  |  DISEASES
6607  |  SMN2  |  DISEASES
6305  |  SBF1  |  DISEASES
6547  |  SLC8A3  |  DISEASES
51091  |  SEPSECS  |  DISEASES
26278  |  SACS  |  DISEASES
2617  |  GARS  |  DISEASES
8502  |  PKP4  |  DISEASES
4099  |  MAG  |  DISEASES
83636  |  C19orf12  |  DISEASES
4287  |  ATXN3  |  DISEASES
2719  |  GPC3  |  DISEASES
174  |  AFP  |  DISEASES
23259  |  DDHD2  |  DISEASES
8091  |  HMGA2  |  DISEASES
6335  |  SCN9A  |  DISEASES
85300  |  ATCAY  |  DISEASES
87178  |  PNPT1  |  DISEASES
7124  |  TNF  |  DISEASES
116228  |  COX20  |  DISEASES
10908  |  PNPLA6  |  DISEASES
3798  |  KIF5A  |  DISEASES
2632  |  GBE1  |  DISEASES
22930  |  RAB3GAP1  |  DISEASES
10243  |  GPHN  |  DISEASES
400916  |  CHCHD10  |  DISEASES
51428  |  DDX41  |  DISEASES
79628  |  SH3TC2  |  DISEASES
4671  |  NAIP  |  DISEASES
4359  |  MPZ  |  DISEASES
65055  |  REEP1  |  DISEASES
9990  |  SLC12A6  |  DISEASES
3316  |  HSPB2  |  DISEASES
820  |  CAMP  |  DISEASES
63895  |  PIEZO2  |  DISEASES
81033  |  KCNH6  |  DISEASES
80347  |  COASY  |  DISEASES
100302692  |  FTX  |  DISEASES
4566  |  MT-TK  |  DISEASES
103752588  |  PACERR  |  DISEASES
Locus(Waiting for update.)
Disease ID 974
Disease axonal neuropathy
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:26)
Disease ID 974
Disease axonal neuropathy
Manually Symptom
UMLS  | Name(Total Manually Symptoms:5)
C1417325  |  multiple sclerosis
C0342783  |  scad deficiency
C0152027  |  sensory disturbances
C0037772  |  spastic paraplegia
C0026847  |  spinal muscular atrophy
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0037772  |  spastic paraplegia  |  4
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1194670031794806155775TDP1umls:C0270921BeFreeThis result provides a direct demonstration that Tdp1 repairs Topo I covalent lesions in vivo and suggests that SCAN1 arises from the recessive neomorphic mutation H493R.0.0019000932007TDP11489993420AG
rs1194670032068749655775TDP1umls:C0270921BeFreeSpinocerebellar ataxia with axonal neuropathy (SCAN 1) is an autosomal recessive disorder caused by a specific point mutation (c.1478A>G, p.H493R) in the tyrosyl-DNA phosphodiesterase (TDP1) gene.0.0019000932010TDP11489993420AG
rs121918312206054529531BAG3umls:C0270921BeFreeWe studied three families with BAG3 p.Pro209Leu mutation showing a severe phenotype of myofibrillar myopathy and axonal neuropathy with giant axons.0.0002714422010BAG310119672373CA,T
rs121918551186287868086AAASumls:C0270921BeFreeAxonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.0.0002714422008AAAS1253308095GA
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)