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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   temporal arteritis
  

Disease ID 418
Disease temporal arteritis
Definition
subacute, granulomatous arteritis involving the external carotid arteries, especially the temporal artery; occurs in elderly persons and may be manifested by constitutional symptoms, particularly severe headache, and sometimes sudden unilateral blindness; shares many of the symptoms of polymyalgia rheumatica.
Synonym
arteritides, temporal
arteritis temporal
arteritis, temporal
ta - temporal arteritis
temporal arteritides
temporal arteritis (disorder)
temporal giant cell arteritis
Orphanet
OMIM
DOID
UMLS
C1956391
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:11)
C0003873  |  rheumatoid arthritis  |  1
C0154723  |  migraine with aura  |  1
C0007117  |  basal cell carcinoma  |  1
C0040028  |  essential thrombocythaemia  |  1
C0040053  |  thrombosis  |  1
C0026764  |  multiple myeloma  |  1
C0040997  |  trigeminal neuralgia  |  1
C0003864  |  arthritis  |  1
C0028841  |  ocular hypotony  |  1
C0032533  |  polymyalgia rheumatica  |  1
C0149931  |  migraine  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
26191  |  PTPN22  |  ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:56)
55024  |  BANK1  |  1.586  |  DISEASES
959  |  CD40LG  |  3.216  |  DISEASES
965  |  CD58  |  1.261  |  DISEASES
9308  |  CD83  |  2.502  |  DISEASES
1025  |  CDK9  |  4.371  |  DISEASES
4283  |  CXCL9  |  1.46  |  DISEASES
1906  |  EDN1  |  1.775  |  DISEASES
26298  |  EHF  |  1.081  |  DISEASES
6624  |  FSCN1  |  1.196  |  DISEASES
3106  |  HLA-B  |  2.106  |  DISEASES
3117  |  HLA-DQA1  |  1.508  |  DISEASES
3123  |  HLA-DRB1  |  4.191  |  DISEASES
3240  |  HP  |  2.679  |  DISEASES
3459  |  IFNGR1  |  1.082  |  DISEASES
3586  |  IL10  |  1.202  |  DISEASES
3605  |  IL17A  |  2.773  |  DISEASES
50615  |  IL21R  |  2.201  |  DISEASES
149233  |  IL23R  |  1.524  |  DISEASES
9235  |  IL32  |  1.544  |  DISEASES
90865  |  IL33  |  1.013  |  DISEASES
3654  |  IRAK1  |  1.5  |  DISEASES
3684  |  ITGAM  |  1.092  |  DISEASES
7044  |  LEFTY2  |  1.514  |  DISEASES
79104  |  MEG8  |  2.912  |  DISEASES
100507436  |  MICA  |  1.108  |  DISEASES
4318  |  MMP9  |  1.456  |  DISEASES
22861  |  NLRP1  |  1.866  |  DISEASES
56138  |  PCDHA11  |  3.14  |  DISEASES
5422  |  POLA1  |  1.547  |  DISEASES
26191  |  PTPN22  |  2.308  |  DISEASES
3921  |  RPSA  |  1.106  |  DISEASES
6283  |  S100A12  |  1.641  |  DISEASES
6288  |  SAA1  |  1.472  |  DISEASES
6401  |  SELE  |  1.718  |  DISEASES
57556  |  SEMA6A  |  1.484  |  DISEASES
12  |  SERPINA3  |  2.228  |  DISEASES
23583  |  SMUG1  |  4.468  |  DISEASES
26774  |  SNORD80  |  2.348  |  DISEASES
6625  |  SNRNP70  |  1.193  |  DISEASES
6775  |  STAT4  |  1.844  |  DISEASES
6818  |  SULT1A3  |  1.788  |  DISEASES
445329  |  SULT1A4  |  1.813  |  DISEASES
6938  |  TCF12  |  1.286  |  DISEASES
6996  |  TDG  |  1.363  |  DISEASES
7099  |  TLR4  |  2.312  |  DISEASES
7100  |  TLR5  |  1.454  |  DISEASES
51284  |  TLR7  |  1.406  |  DISEASES
54106  |  TLR9  |  1.188  |  DISEASES
7124  |  TNF  |  2.967  |  DISEASES
7133  |  TNFRSF1B  |  2.539  |  DISEASES
8718  |  TNFRSF25  |  1.871  |  DISEASES
3604  |  TNFRSF9  |  1.196  |  DISEASES
10673  |  TNFSF13B  |  1.435  |  DISEASES
27229  |  TUBGCP4  |  1.658  |  DISEASES
9094  |  UNC119  |  1.416  |  DISEASES
7417  |  VDAC2  |  1.681  |  DISEASES
Locus(Waiting for update.)
Disease ID 418
Disease temporal arteritis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:3)
HP:0008030  |  Retinal arteritis
HP:0003565  |  Elevated sedimentation rate
HP:0000618  |  Blindness
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:13)
HP:0002315  |  Headaches  |  4
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0002077  |  Migraine with aura  |  1
HP:0100661  |  Trigeminal neuralgia  |  1
HP:0012474  |  Obstructed carotid artery  |  1
HP:0001369  |  Arthritis  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0003565  |  Elevated sedimentation rate  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0002671  |  Basalioma  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0030164  |  Jaw claudication  |  1
Disease ID 418
Disease temporal arteritis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:57)
C2700511  |  erythroleukemia
C2240374  |  eosinophilia
C2168170  |  leg claudication
C2096315  |  headache
C2073625  |  pleural effusion
C2046121  |  aortic dissection
C2029884  |  hearing loss
C1963736  |  tongue necrosis
C1963154  |  renal failure
C1962966  |  retinopathy
C1879328  |  bilateral blindness
C1562901  |  peripheral ulcerative keratitis
C1402315  |  vascular lesions
C1336970  |  visual manifestations
C1304164  |  generalized granuloma annulare
C1290884  |  inflammatory disease
C1253936  |  synovial effusion
C1180561  |  internal elastic lamina
C1148477  |  sudden deafness
C1000483  |  anemia
C0836924  |  thrombocytosis
C0752303  |  urological manifestations
C0522224  |  palsy
C0521516  |  polymyalgia
C0517555  |  venous thrombosis
C0456909  |  loss of vision
C0456909  |  blindness
C0344232  |  blurred vision
C0339731  |  charles bonnet syndrome
C0271240  |  unilateral blindness
C0239819  |  hand edema
C0234362  |  synkinesis
C0231243  |  early complication
C0221390  |  marantic endocarditis
C0162323  |  polyarthritis
C0155339  |  brown syndrome
C0039483  |  giant cell arteritis
C0037284  |  skin lesions
C0037090  |  respiratory symptoms
C0036454  |  visual field loss
C0036454  |  visual field defects
C0036220  |  kaposi's sarcoma
C0031117  |  peripheral neuropathy
C0030167  |  pachymeningitis
C0029118  |  opportunistic infections
C0027726  |  nephrotic syndrome
C0022658  |  renal disease
C0022116  |  ischemia
C0021845  |  intestinal perforation
C0021308  |  infarction
C0020676  |  hypothyroidism
C0020635  |  hypopituitarism
C0020550  |  hyperthyroidism
C0019937  |  horner's syndrome
C0017086  |  gangrene
C0007688  |  central retinal artery occlusion
C0007286  |  carpal tunnel syndrome
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:7)
C0018681  |  headache  |  3
C0521516  |  polymyalgia  |  2
C0014457  |  eosinophilia  |  1
C1180561  |  internal elastic lamina  |  1
C1963736  |  tongue necrosis  |  1
C0037284  |  skin lesions  |  1
C0042487  |  venous thrombosis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs188383220682661958CD40umls:C1956391GAD[Our results suggest a potential implication of the CD40 rs1883832 C/T polymorphism in susceptibility to visual ischemic manifestations in individuals with biopsy-proven GCA.]0.0023670322010CD402046118343TC
rs2104286208105073559IL2RAumls:C1956391GAD[IL2RA rs2104286 polymorphism does not appear to be a genetic risk factor for susceptibility to biopsy-proven GCA. Also, this polymorphism does not seem to be implicated in the clinical expression of this vasculitis.]0.0023670322010IL2RA106057082TC
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0003565Elevated erythrocyte sedimentation rateMP:0008770decreased survivor ratea smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls
Mapped by homologous gene(Total Items:3)
HP ID HP Name MP ID MP Name Annotation
HP:0000618BlindnessMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0003565Elevated erythrocyte sedimentation rateMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0008030Retinal arteritisMP:0010850increased effector memory CD8-positive, alpha-beta T cell numberincreased number of CD8-positive, alpha beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative
Disease ID 418
Disease temporal arteritis
Case(Waiting for update.)