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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   lead poisoning
  

Disease ID 1560
Disease lead poisoning
Definition
Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds.
Synonym
lead - toxic effect
lead and lead compounds causing toxic effect
lead and lead compounds causing toxic effect (disorder)
lead compound causing toxic effect nos
lead compound causing toxic effect nos (disorder)
lead compound poisoning
lead compound poisoning (disorder)
lead pois
lead poison
lead poisoning [disease/finding]
lead poisonings
plumbism
pois lead
poisoning by compounds of lead
poisoning, lead
poisonings, lead
saturnine poisoning
saturnism
tox eff lead compnd nos
toxic effect of lead and its compounds
toxic effect of lead and its compounds (including fumes)
toxic effect of lead and its compounds, including fumes
toxic effect of lead compound
toxic effect of lead compound (disorder)
toxic effect of lead compound, nos
toxic effect of unspecified lead compound
Orphanet
UMLS
C0023176
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:9)
C0154652  |  eosinophilic meningitis  |  1
C0242350  |  erectile dysfunction  |  1
C0000786  |  miscarriage  |  1
C0011570  |  depression  |  1
C0018099  |  gout  |  1
C0009806  |  constipation  |  1
C0002871  |  anemia  |  1
C0011847  |  diabetes  |  1
C0442874  |  neuropathy  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:6)
210  |  ALAD  |  CTD_human
4318  |  MMP9  |  CTD_human
3077  |  HFE  |  CTD_human
7517  |  XRCC3  |  CTD_human
7421  |  VDR  |  CTD_human
84560  |  MT4  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:7)
210  |  ALAD  |  CIPHER;CTD_human
4524  |  MTHFR  |  CIPHER
7421  |  VDR  |  CIPHER;CTD_human
7517  |  XRCC3  |  CTD_human
4318  |  MMP9  |  CTD_human
3077  |  HFE  |  CTD_human
84560  |  MT4  |  CTD_human
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1560
Disease lead poisoning
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:13)
HP:0001903  |  Anemia  |  2
HP:0002019  |  Dyschezia  |  1
HP:0001622  |  Premature delivery  |  1
HP:0012450  |  Chronic constipation  |  1
HP:0001997  |  Gout  |  1
HP:0000716  |  Depression  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0011848  |  Abdominal colic  |  1
HP:0012531  |  Pain  |  1
HP:0000802  |  Erectile dysfunction  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0001824  |  Weight loss  |  1
Disease ID 1560
Disease lead poisoning
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1801133205049794524MTHFRumls:C0023176GAD[The maternal MTHFR 677T allele is an independent predictor of poorer child neurodevelopment at 24 mo. These results suggest that maternal genetic variations in folate metabolism during pregnancy may program offspring neurodevelopment trajectories. Further]0.0023670322010MTHFR111796321GA
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 1560
Disease lead poisoning
Case(Waiting for update.)