Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   pyomyositis
  

Disease ID 487
Disease pyomyositis
Definition
A suppurative infection of muscle.
Synonym
myositis, tropical
pyomyositis, tropical
tropical myositis
tropical pyomyositis
tropical pyomyositis (disorder)
tropical pyomyositis [dup] (disorder)
Orphanet
DOID
UMLS
C0041188
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:17)
C0270629  |  epidural abscess  |  4
C0003864  |  arthritis  |  3
C0029443  |  osteomyelitis  |  3
C0003874  |  septic arthritis  |  2
C0409974  |  lupus erythematosus  |  2
C0009492  |  compartment syndrome  |  2
C0024141  |  systemic lupus erythematosus  |  2
C1704437  |  respiratory distress syndrome  |  1
C0476089  |  endometrial ca  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0040896  |  trichinellosis  |  1
C0037054  |  sickle cell trait  |  1
C0027121  |  myositis  |  1
C0011847  |  diabetes  |  1
C0034065  |  pulmonary embolism  |  1
C0011849  |  diabetes mellitus  |  1
C0476089  |  endometrial cancer  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:14)
1645  |  AKR1C1  |  2.301  |  DISEASES
996  |  CDC27  |  3.618  |  DISEASES
1378  |  CR1  |  1.467  |  DISEASES
2157  |  F8  |  1.448  |  DISEASES
2214  |  FCGR3A  |  1.209  |  DISEASES
2875  |  GPT  |  2.997  |  DISEASES
3329  |  HSPD1  |  1.673  |  DISEASES
4151  |  MB  |  1.337  |  DISEASES
79104  |  MEG8  |  2.523  |  DISEASES
3164  |  NR4A1  |  2.231  |  DISEASES
83695  |  RHNO1  |  1.801  |  DISEASES
6164  |  RPL34  |  2.451  |  DISEASES
8801  |  SUCLG2  |  2.804  |  DISEASES
7137  |  TNNI3  |  1.364  |  DISEASES
Locus(Waiting for update.)
Disease ID 487
Disease pyomyositis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:12)
HP:0100616  |  Testicular teratoma
HP:0001974  |  Leukocytosis
HP:0003326  |  Myalgia
HP:0001645  |  Sudden cardiac death
HP:0100838  |  Recurrent cutaneous abscess formation
HP:0001482  |  Subcutaneous nodule
HP:0001824  |  Weight loss
HP:0001945  |  Fever
HP:0100806  |  Sepsis
HP:0002719  |  Recurrent infections
HP:0100614  |  Myositis
HP:0000083  |  Renal insufficiency
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:14)
HP:0001369  |  Arthritis  |  3
HP:0002754  |  Bone infection  |  3
HP:0100806  |  Sepsis  |  2
HP:0003095  |  Septic arthritis  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0003326  |  Muscle pain  |  2
HP:0100614  |  Muscle inflammation  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0000969  |  Dropsy  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0001945  |  Fever  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0012531  |  Pain  |  1
Disease ID 487
Disease pyomyositis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:6)
C2364133  |  infection
C0600327  |  toxic shock syndrome
C0458224  |  piriformis muscle syndrome
C0264008  |  anterior tibial compartment syndrome
C0015645  |  fasciitis
C0006105  |  brain abscesses
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0009450  |  infection  |  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:3)
HP ID HP Name MP ID MP Name Annotation
HP:0000083Renal insufficiencyMP:0003335exocrine pancreatic insufficiencyinadequate synthesis and/or secretion of digestive enzymes by the exocrine portion of the pancreas, usually due to loss of acinar tissue from idiopathic atrophy or acute or chronic inflammation, causing maldigestion and malabsorption of nutrients
HP:0001824Weight lossMP:0005114premature hair lossrelease of fur at an earlier than expected time
HP:0001645Sudden cardiac deathMP:0012557decreased calcium uptake by cardiac muscledecreased directed movement of calcium ions into cardiac muscle; decreased or disrupted uptake may give rise to energetic deficit and oxidative stress. leading to cardiac disease
Mapped by homologous gene(Total Items:11)
HP ID HP Name MP ID MP Name Annotation
HP:0100614MyositisMP:0011635abnormal mitochondrial crista morphologyAny of the inward folds of the mitochondrial inner membrane; crista number, extent, and shape differ in mitochondria from different tissues and organisms; crista appear to be devices for increasing the surface area of the mitochondrial inner membrane, whe
HP:0100806SepsisMP:0011708decreased fibroblast cell migrationreduced frequency of or less rapid fibroblast cell migration that is accomplished by extension and retraction of a fibroblast pseudopodium
HP:0001945FeverMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0001824Weight lossMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0002719Recurrent infectionsMP:0020234decreased basal metabolismdecrease in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state
HP:0100838Recurrent cutaneous abscess formationMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000083Renal insufficiencyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0001974LeukocytosisMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0001645Sudden cardiac deathMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
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(+).
Disease ID 487
Disease pyomyositis
Case(Waiting for update.)