Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   cutaneous leukocytoclastic angiitis
  

Disease ID 1121
Disease cutaneous leukocytoclastic angiitis
Definition
Disorder characterized by a vasculitic syndrome associated with exposure to an antigen such as a drug, infectious agent, or other foreign or endogenous substance. Its pathophysiology includes immune complex deposition and a wide range of skin lesions. Hypersensitivity or allergy is present in some but not all cases.
Synonym
allergic cutaneous angiitides
allergic cutaneous angiitis
allergic cutaneous vasculitides
allergic cutaneous vasculitis
allergic vasculitides, cutaneous
allergic vasculitis
allergic vasculitis, cutaneous
angiitides, allergic cutaneous
angiitides, cutaneous leukocytoclastic
angiitides, hypersensitivity
angiitis, allergic cutaneous
angiitis, cutaneous leukocytoclastic
angiitis, hypersensitivity
angiitis, leukocytoclastic
cutaneous allergic vasculitides
cutaneous allergic vasculitis
cutaneous angiitides, allergic
cutaneous angiitis, allergic
cutaneous hypersensitivity vasculitis
cutaneous leucocytoclastic angiitis
cutaneous leukocytoclastic angiitides
cutaneous leukocytoclastic angiitis (disorder)
cutaneous leukocytoclastic vasculitides
cutaneous leukocytoclastic vasculitis
cutaneous small vessel vasculitis
cutaneous vasculitides, allergic
cutaneous vasculitis, allergic
hypersensit angiitis nos
hypersensitivity angiitides
hypersensitivity angiitis
hypersensitivity angiitis (disorder)
hypersensitivity angiitis nos
hypersensitivity angiitis nos (disorder)
hypersensitivity angiitis, unspecified
hypersensitivity vasculitides
hypersensitivity vasculitis
leucocytoclastic angiitis
leucocytoclastic vasculitis
leukocytoclastic angiitides, cutaneous
leukocytoclastic angiitis
leukocytoclastic angiitis, cutaneous
leukocytoclastic vasculitides, cutaneous
leukocytoclastic vasculitis
leukocytoclastic vasculitis, cutaneous
maladie trisymptome
trisymptome
vasculitides, allergic cutaneous
vasculitides, cutaneous allergic
vasculitides, cutaneous leukocytoclastic
vasculitides, hypersensitivity
vasculitis allergic
vasculitis leukocytoclastic
vasculitis nonspecific allergic
vasculitis nonspecific allergic hypersensitivity vasculitis
vasculitis, allergic
vasculitis, allergic cutaneous
vasculitis, cutaneous allergic
vasculitis, cutaneous leukocytoclastic
vasculitis, hypersensitivity
vasculitis, leukocytoclastic
vasculitis, leukocytoclastic, cutaneous
vasculitis, leukocytoclastic, cutaneous [disease/finding]
Orphanet
DOID
ICD10
UMLS
C0151436
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:49)
C0034150  |  purpura  |  6
C0042384  |  vasculitis  |  5
C0041296  |  tuberculosis  |  2
C0021390  |  inflammatory bowel disease  |  2
C0011603  |  dermatitis  |  2
C0151436  |  leukocytoclastic vasculitis  |  2
C0009324  |  ulcerative colitis  |  2
C0409974  |  lupus erythematosus  |  1
C0009319  |  colitis  |  1
C0026764  |  myeloma  |  1
C0376545  |  hematological malignancies  |  1
C0034152  |  schonlein-henoch purpura  |  1
C0014121  |  bacterial endocarditis  |  1
C0024299  |  lymphoma  |  1
C0001418  |  adenocarcinoma  |  1
C0026934  |  mycoplasma  |  1
C0699790  |  colon carcinoma  |  1
C0151436  |  hypersensitivity vasculitis  |  1
C0010403  |  cryoglobulinemia  |  1
C0021831  |  bowel disease  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0011608  |  dermatitis herpetiformis  |  1
C0022081  |  iritis  |  1
C0030326  |  panniculitis  |  1
C0042769  |  virus infection  |  1
C0034152  |  henoch-schonlein purpura  |  1
C0026764  |  multiple myeloma  |  1
C0040053  |  thrombosis  |  1
C0040028  |  essential thrombocythaemia  |  1
C0699790  |  carcinoma of the colon  |  1
C0042900  |  vitiligo  |  1
C0024137  |  cutaneous lupus erythematosus  |  1
C0021400  |  influenza  |  1
C0497327  |  dementia  |  1
C0014118  |  endocarditis  |  1
C0007134  |  hypernephroma  |  1
C0003873  |  rheumatoid arthritis  |  1
C0019360  |  herpes zoster  |  1
C0270922  |  demyelinating polyneuropathy  |  1
C0010346  |  crohn's disease  |  1
C0034152  |  henoch purpura  |  1
C0019348  |  herpes simplex  |  1
C0743039  |  progressive dementia  |  1
C0004623  |  bacterial infection  |  1
C0162529  |  ischemic colitis  |  1
C0007113  |  rectal cancer  |  1
C0024623  |  gastric cancer  |  1
C0038013  |  ankylosing spondylitis  |  1
C0338106  |  adenocarcinoma of the colon  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:47)
56  |  ACRV1  |  1.203  |  DISEASES
183  |  AGT  |  1.535  |  DISEASES
545  |  ATR  |  1.88  |  DISEASES
567  |  B2M  |  1.09  |  DISEASES
720  |  C4A  |  2.996  |  DISEASES
721  |  C4B  |  2.315  |  DISEASES
728  |  C5AR1  |  1.564  |  DISEASES
959  |  CD40LG  |  4.024  |  DISEASES
1471  |  CST3  |  1.549  |  DISEASES
1589  |  CYP21A2  |  1.086  |  DISEASES
5169  |  ENPP3  |  1.436  |  DISEASES
83715  |  ESPN  |  1.612  |  DISEASES
355  |  FAS  |  1.051  |  DISEASES
2204  |  FCAR  |  1.293  |  DISEASES
2224  |  FDPS  |  1.466  |  DISEASES
389549  |  FEZF1  |  1.275  |  DISEASES
26762  |  HAVCR1  |  1.275  |  DISEASES
3106  |  HLA-B  |  1.745  |  DISEASES
3123  |  HLA-DRB1  |  2.605  |  DISEASES
3320  |  HSP90AA1  |  4.436  |  DISEASES
3586  |  IL10  |  1.573  |  DISEASES
3605  |  IL17A  |  2.237  |  DISEASES
29949  |  IL19  |  1.938  |  DISEASES
3572  |  IL6ST  |  1.169  |  DISEASES
64423  |  INF2  |  1.427  |  DISEASES
3920  |  LAMP2  |  1.343  |  DISEASES
4153  |  MBL2  |  1.297  |  DISEASES
4192  |  MDK  |  1.925  |  DISEASES
4318  |  MMP9  |  1.211  |  DISEASES
114548  |  NLRP3  |  1.066  |  DISEASES
5076  |  PAX2  |  1.25  |  DISEASES
5277  |  PIGA  |  2.274  |  DISEASES
23556  |  PIGN  |  2.728  |  DISEASES
5420  |  PODXL  |  2.166  |  DISEASES
26191  |  PTPN22  |  1.003  |  DISEASES
7732  |  RNF112  |  1.123  |  DISEASES
6401  |  SELE  |  2.532  |  DISEASES
5265  |  SERPINA1  |  1.731  |  DISEASES
169981  |  SPIN3  |  3.248  |  DISEASES
129685  |  TAF8  |  1.684  |  DISEASES
80222  |  TARS2  |  1.833  |  DISEASES
123283  |  TARSL2  |  1.869  |  DISEASES
7056  |  THBD  |  1.44  |  DISEASES
7099  |  TLR4  |  1.654  |  DISEASES
7124  |  TNF  |  2.321  |  DISEASES
7133  |  TNFRSF1B  |  1.628  |  DISEASES
7148  |  TNXB  |  1.135  |  DISEASES
Locus(Waiting for update.)
Disease ID 1121
Disease cutaneous leukocytoclastic angiitis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:14)
HP:0000988  |  Skin rash
HP:0001025  |  Urticaria
HP:0002829  |  Arthralgia
HP:0010783  |  Erythema
HP:0000965  |  Cutis marmorata
HP:0002633  |  Vasculitis
HP:0003326  |  Myalgia
HP:0000163  |  Abnormality of the oral cavity
HP:0001482  |  Subcutaneous nodule
HP:0001945  |  Fever
HP:0100758  |  Gangrene
HP:0000979  |  Purpura
HP:0200034  |  Papule
HP:0001581  |  Recurrent skin infections
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:26)
HP:0000979  |  Purpura  |  6
HP:0002633  |  Vasculitis  |  5
HP:0100279  |  Ulcerative colitis  |  2
HP:0010783  |  Erythema  |  2
HP:0005584  |  Renal cell carcinoma  |  1
HP:0030731  |  Carcinoma  |  1
HP:0002583  |  Colitis  |  1
HP:0005549  |  Low blood neutrophil level since birth  |  1
HP:0012490  |  Inflammation of fat tissue  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0006775  |  Multiple myeloma  |  1
HP:0003565  |  Elevated sedimentation rate  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0002665  |  Lymphoma  |  1
HP:0040276  |  Adenocarcinoma of the colon  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0100778  |  Cryoglobulinemia  |  1
HP:0200029  |  Cutaneous vasculitis  |  1
HP:0001101  |  Iritis  |  1
HP:0000726  |  Dementia  |  1
HP:0000969  |  Dropsy  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0001045  |  Blotchy loss of skin color  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0002829  |  Arthralgias  |  1
Disease ID 1121
Disease cutaneous leukocytoclastic angiitis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0034150  |  purpura  |  6
C0009324  |  ulcerative colitis  |  2
C0010403  |  cryoglobulinemia  |  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:2)
HP ID HP Name MP ID MP Name Annotation
HP:0001581Recurrent skin infectionsMP:0009932skin fibrosisinvasion of fibrous connective tissue into the skin, often resulting from inflammation or injury
HP:0000163Abnormality of the oral cavityMP:0009657failure of chorioallantoic fusionfailure to initiate and/or complete the formation of a highly vascularized extra-embryonic fetal membrane by fusion of the chorion and allantois
Mapped by homologous gene(Total Items:14)
HP ID HP Name MP ID MP Name Annotation
HP:0200034PapuleMP:0013745abnormal eyelid margin morphologyany structural anomaly of the confluence of the mucosal surface of the conjunctiva, the edge of the orbicularis, and the cutaneous epithelium
HP:0001945FeverMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0002829ArthralgiaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0000979PurpuraMP:0020216decreased circulating complement protein levelless than normal levels of the serum proteins that act sequentially to allow for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes
HP:0001581Recurrent skin infectionsMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0010783ErythemaMP:0013781abnormal mammary gland luminal epithelium morphologyany structural anomaly of the inner cell layer of the mammary epithelium bilayer that lines the luminal surface of mammary gland ducts and alveoli; luminal cells have only limited contact with the underlying basement membrane and surrounding connective ti
HP:0001025UrticariaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0002633VasculitisMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0000163Abnormality of the oral cavityMP:0013501increased fibroblast apoptosisincrease in the timing or the number of fibroblast cells undergoing programmed cell death
HP:0001482Subcutaneous noduleMP:0013542abnormal submandibular gland branching morphogenesis
HP:0003326MyalgiaMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
HP:0000965Cutis marmorataMP:0014179abnormal blood-retinal barrier functionanomaly in the function of the part of the blood-ocular barrier that consists of cells that are joined tightly together to prevent certain substances from entering the tissue of the retina; the BRB consists of non-fenestrated capillaries of the retinal ci
HP:0100758GangreneMP:0011517hyperoxaluriaabnormally high levels of oxalic acid or oxalates in the urine; many metal ions form insoluble precipitates with oxalate, a prominent example being calcium oxalate, the primary constituent of the most common kind of kidney stones
HP:0000988Skin rashMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
Disease ID 1121
Disease cutaneous leukocytoclastic angiitis
Case(Waiting for update.)