Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   lichen planus
  

Disease ID 715
Disease lichen planus
Definition
An inflammatory, pruritic disease of the skin and mucous membranes, which can be either generalized or localized. It is characterized by distinctive purplish, flat-topped papules having a predilection for the trunk and flexor surfaces. The lesions may be discrete or coalesce to form plaques. Histologically, there is a "saw-tooth" pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal inflammatory infiltrate composed predominantly of T-cells. Etiology is unknown.
Synonym
lichen planus (disorder)
lichen planus [disease/finding]
lichen planus nos
lichen planus nos (disorder)
lichen ruber planus
lichen rubra planus
lichen, ruber planus
lp - lichen planus
ruber planus
DOID
UMLS
C0023646
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:42)
C0019196  |  hepatitis c  |  9
C0019158  |  hepatitis  |  8
C0003467  |  anxiety  |  5
C0042769  |  virus infection  |  5
C0017574  |  gingivitis  |  4
C0011570  |  depression  |  3
C0021053  |  immune disease  |  3
C0007137  |  squamous cell carcinoma  |  2
C0019163  |  hepatitis b  |  2
C0040128  |  thyroid disease  |  2
C0948265  |  metabolic syndrome  |  2
C0008049  |  varicella  |  1
C0006840  |  candidosis  |  1
C0026896  |  myasthenia gravis  |  1
C0221027  |  good syndrome  |  1
C1568868  |  oral mucositis  |  1
C0376480  |  gingival enlargement  |  1
C0032580  |  polyposis coli  |  1
C0155550  |  neural deafness  |  1
C0032580  |  adenomatous polyposis coli  |  1
C0006849  |  oral candidosis  |  1
C0006840  |  candidiasis  |  1
C0026640  |  oral cancer  |  1
C0040100  |  thymoma  |  1
C0265334  |  pachyonychia congenita  |  1
C0022572  |  keratoacanthomas  |  1
C0022593  |  keratosis  |  1
C0039128  |  syphilis  |  1
C0013415  |  dysthymia  |  1
C0006840  |  candida infection  |  1
C0375071  |  vulvar cancer  |  1
C0162839  |  porokeratosis  |  1
C0026769  |  multiple sclerosis  |  1
C0007570  |  celiac disease  |  1
C0018784  |  sensorineural deafness  |  1
C0346054  |  verruciform xanthoma  |  1
C0019360  |  zoster  |  1
C0002170  |  alopecia  |  1
C0206706  |  verrucous carcinoma  |  1
C0085253  |  adult-onset still's disease  |  1
C0031099  |  periodontitis  |  1
C0036202  |  sarcoidosis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
3123  |  HLA-DRB1  |  CIPHER
7124  |  TNF  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:112)
11173  |  ADAMTS7  |  1.383  |  DISEASES
276  |  AMY1A  |  1.044  |  DISEASES
277  |  AMY1B  |  1.044  |  DISEASES
278  |  AMY1C  |  1.044  |  DISEASES
481  |  ATP1B1  |  1.575  |  DISEASES
488  |  ATP2A2  |  2.345  |  DISEASES
538  |  ATP7A  |  1.183  |  DISEASES
283149  |  BCL9L  |  1.603  |  DISEASES
9184  |  BUB3  |  1.442  |  DISEASES
59082  |  CARD18  |  2.801  |  DISEASES
6364  |  CCL20  |  1.242  |  DISEASES
910  |  CD1B  |  1.755  |  DISEASES
914  |  CD2  |  1.717  |  DISEASES
50489  |  CD207  |  2.373  |  DISEASES
51744  |  CD244  |  1.104  |  DISEASES
29126  |  CD274  |  2.137  |  DISEASES
958  |  CD40  |  1.017  |  DISEASES
959  |  CD40LG  |  3.43  |  DISEASES
960  |  CD44  |  1.292  |  DISEASES
965  |  CD58  |  1.981  |  DISEASES
1029  |  CDKN2A  |  1.988  |  DISEASES
1041  |  CDSN  |  1.791  |  DISEASES
387836  |  CLEC2A  |  2.041  |  DISEASES
170482  |  CLEC4C  |  2.584  |  DISEASES
1308  |  COL17A1  |  4.527  |  DISEASES
10087  |  COL4A3BP  |  1.765  |  DISEASES
1294  |  COL7A1  |  1.733  |  DISEASES
64109  |  CRLF2  |  1.507  |  DISEASES
4283  |  CXCL9  |  3.311  |  DISEASES
2833  |  CXCR3  |  3.124  |  DISEASES
1565  |  CYP2D6  |  1.35  |  DISEASES
100289462  |  DEFB4B  |  2.383  |  DISEASES
1832  |  DSP  |  2.614  |  DISEASES
7957  |  EPM2A  |  1.267  |  DISEASES
356  |  FASLG  |  2.108  |  DISEASES
2214  |  FCGR3A  |  2.232  |  DISEASES
389549  |  FEZF1  |  1.026  |  DISEASES
2312  |  FLG  |  3.072  |  DISEASES
388698  |  FLG2  |  2.213  |  DISEASES
2316  |  FLNA  |  2.011  |  DISEASES
342184  |  FMN1  |  1.655  |  DISEASES
50943  |  FOXP3  |  2.985  |  DISEASES
2625  |  GATA3  |  1.276  |  DISEASES
392862  |  GRID2IP  |  2.304  |  DISEASES
51696  |  HECA  |  1.16  |  DISEASES
3105  |  HLA-A  |  1.113  |  DISEASES
3106  |  HLA-B  |  1.137  |  DISEASES
3107  |  HLA-C  |  1.504  |  DISEASES
3329  |  HSPD1  |  1.064  |  DISEASES
3339  |  HSPG2  |  1.272  |  DISEASES
8692  |  HYAL2  |  1.029  |  DISEASES
3440  |  IFNA2  |  1.455  |  DISEASES
3456  |  IFNB1  |  1.345  |  DISEASES
8518  |  IKBKAP  |  1.374  |  DISEASES
3586  |  IL10  |  2.36  |  DISEASES
3605  |  IL17A  |  2.643  |  DISEASES
50616  |  IL22  |  1.179  |  DISEASES
3563  |  IL3RA  |  2.649  |  DISEASES
22801  |  ITGA11  |  2.142  |  DISEASES
3683  |  ITGAL  |  2.185  |  DISEASES
3684  |  ITGAM  |  1.323  |  DISEASES
3713  |  IVL  |  3.317  |  DISEASES
8242  |  KDM5C  |  1.018  |  DISEASES
547  |  KIF1A  |  1.054  |  DISEASES
3812  |  KIR3DL2  |  1.227  |  DISEASES
440900  |  LINC01191  |  2.857  |  DISEASES
4014  |  LOR  |  2.395  |  DISEASES
64900  |  LPIN3  |  1.869  |  DISEASES
80059  |  LRRTM4  |  2.709  |  DISEASES
2315  |  MLANA  |  2.196  |  DISEASES
27030  |  MLH3  |  1.066  |  DISEASES
4312  |  MMP1  |  1.474  |  DISEASES
4318  |  MMP9  |  1.907  |  DISEASES
4599  |  MX1  |  2.868  |  DISEASES
594857  |  NPS  |  1.174  |  DISEASES
2516  |  NR5A1  |  2.381  |  DISEASES
9542  |  NRG2  |  1.575  |  DISEASES
4942  |  OAT  |  1.908  |  DISEASES
4946  |  OAZ1  |  1.809  |  DISEASES
80380  |  PDCD1LG2  |  2.425  |  DISEASES
5178  |  PEG3  |  1.008  |  DISEASES
5339  |  PLEC  |  2.225  |  DISEASES
6490  |  PMEL  |  1.402  |  DISEASES
5493  |  PPL  |  2.902  |  DISEASES
9374  |  PPT2  |  1.072  |  DISEASES
5743  |  PTGS2  |  1.582  |  DISEASES
201475  |  RAB12  |  1.996  |  DISEASES
6014  |  RIT2  |  2.044  |  DISEASES
6097  |  RORC  |  1.552  |  DISEASES
58490  |  RPRD1B  |  2.057  |  DISEASES
6280  |  S100A9  |  1.859  |  DISEASES
6401  |  SELE  |  1.988  |  DISEASES
6663  |  SOX10  |  1.001  |  DISEASES
6677  |  SPAM1  |  1.023  |  DISEASES
9901  |  SRGAP3  |  1.491  |  DISEASES
54879  |  ST7L  |  2.983  |  DISEASES
6863  |  TAC1  |  1.914  |  DISEASES
129685  |  TAF8  |  1.346  |  DISEASES
126637  |  TCHHL1  |  3.035  |  DISEASES
7072  |  TIA1  |  2.123  |  DISEASES
114609  |  TIRAP  |  1.928  |  DISEASES
7096  |  TLR1  |  2.358  |  DISEASES
7099  |  TLR4  |  2.331  |  DISEASES
51284  |  TLR7  |  1.544  |  DISEASES
54106  |  TLR9  |  1.612  |  DISEASES
7124  |  TNF  |  3.778  |  DISEASES
8784  |  TNFRSF18  |  1.272  |  DISEASES
7133  |  TNFRSF1B  |  2.2  |  DISEASES
8718  |  TNFRSF25  |  2.151  |  DISEASES
85480  |  TSLP  |  1.721  |  DISEASES
9094  |  UNC119  |  1.111  |  DISEASES
7422  |  VEGFA  |  1.439  |  DISEASES
Locus(Waiting for update.)
Disease ID 715
Disease lichen planus
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:33)
HP:0012115  |  Liver inflammation  |  9
HP:0000739  |  Anxiety  |  5
HP:0000230  |  Inflamed gums  |  5
HP:0030731  |  Carcinoma  |  3
HP:0000716  |  Depression  |  3
HP:0002960  |  Autoimmune condition  |  3
HP:0002745  |  Oral idiopathic leukoplakia  |  2
HP:0100699  |  Scarring  |  2
HP:0012531  |  Pain  |  2
HP:0002860  |  Squamous cell carcinoma  |  2
HP:0001596  |  Hair loss  |  2
HP:0200123  |  Chronic liver inflammation  |  2
HP:0000820  |  Thyroid abnormality  |  2
HP:0008404  |  Dystrophic nails  |  1
HP:0200120  |  Chronic active hepatitis  |  1
HP:0002608  |  Celiac disease  |  1
HP:0100522  |  Thymoma  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0000989  |  pruritis  |  1
HP:0010783  |  Erythema  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0000212  |  Gingival overgrowth  |  1
HP:0003764  |  Naevus  |  1
HP:0000407  |  sensorineural hearing loss  |  1
HP:0002043  |  Esophageal stricture  |  1
HP:0007418  |  Alopecia totalis  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0008066  |  Skin bullae  |  1
HP:0008527  |  Hearing loss, congenital sensorineural  |  1
HP:0200016  |  Acral keratosis  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0200044  |  Porokeratosis  |  1
Disease ID 715
Disease lichen planus
Manually Symptom
UMLS  | Name(Total Manually Symptoms:38)
C2364133  |  infection
C2186532  |  liver disease
C1420725  |  thymoma
C1290886  |  chronic inflammatory disease
C1274790  |  cicatrizing conjunctivitis
C0878500  |  epithelial dysplasia
C0850666  |  h. pylori infection
C0849640  |  skin damage
C0520463  |  active chronic hepatitis
C0451641  |  urolithiasis
C0409974  |  lupus erythematosus
C0406443  |  twenty-nail dystrophy
C0271650  |  glucose intolerance
C0235401  |  abnormal glucose tolerance
C0221260  |  nail dystrophy
C0220847  |  hepatitis c
C0220641  |  oral cancer
C0151546  |  oral carcinomas
C0086873  |  scarring alopecia
C0042900  |  vitiligo
C0042769  |  virus infection
C0041408  |  turner's syndrome
C0037285  |  skin manifestations
C0037284  |  skin lesions
C0033860  |  psoriasis
C0033774  |  pruritus
C0030805  |  bullous pemphigoid
C0029166  |  oral manifestations
C0029166  |  oral manifestation
C0024141  |  le syndrome
C0022906  |  canalicular obstruction
C0022573  |  keratoconjunctivitis
C0022572  |  keratoacanthoma
C0021053  |  immune disorder
C0017677  |  benign migratory glossitis
C0017577  |  desquamative gingivitis
C0014866  |  oesophageal stricture
C0009763  |  conjunctivitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:10)
C0009450  |  infection  |  11
C0019196  |  hepatitis c  |  9
C0042769  |  virus infection  |  5
C0037284  |  skin lesions  |  2
C0017577  |  desquamative gingivitis  |  2
C0037285  |  skin manifestations  |  1
C0221260  |  nail dystrophy  |  1
C0033774  |  pruritus  |  1
C0040100  |  thymoma  |  1
C0026640  |  oral cancer  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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.)
Disease ID 715
Disease lichen planus
Case(Waiting for update.)