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PedAM

Pediatric Disease Annotations & Medicines



   factitious disorder
  

Disease ID 1855
Disease factitious disorder
Definition
Disorders characterized by physical or psychological symptoms that are not real, genuine, or natural.
Synonym
[x]intentional production or feigning of symptoms or disabilities, either physical or psychological [factitious disorder]
[x]intentional production or feigning of symptoms or disabilities, either physical or psychological [factitious disorder] (disorder)
disorder factitious
disorders, factitious
factitious dis
factitious disorder (disorder)
factitious disorder nos
factitious disorder, nos
factitious disorders
factitious disorders [disease/finding]
factitious illness
DOID
UMLS
C0015480
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:5)
C0030567  |  parkinson's disease  |  1
C0037650  |  somatoform disorder  |  1
C0853193  |  bipolar i disorder  |  1
C0030567  |  idiopathic parkinson's disease  |  1
C0010346  |  crohn's disease  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:10)
2645  |  GCK  |  DISEASES
56269  |  IRGC  |  DISEASES
3630  |  INS  |  DISEASES
51181  |  DCXR  |  DISEASES
4968  |  OGG1  |  DISEASES
8630  |  HSD17B6  |  DISEASES
3767  |  KCNJ11  |  DISEASES
6833  |  ABCC8  |  DISEASES
7018  |  TF  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1855
Disease factitious disorder
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:7)
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0001304  |  Dystonia musculorum deformans  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0012166  |  Skin-picking  |  1
HP:0002105  |  Hemoptysis  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
Disease ID 1855
Disease factitious disorder
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining 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.)
Chemical(Total Drugs:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0015480propranololD011433525-66-6factitious disordersMESH:D005162marker/mechanism436541
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)