Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   hypervitaminosis a
  

Disease ID 1565
Disease hypervitaminosis a
Definition
A symptom complex resulting from ingesting excessive amounts of VITAMIN A.
Synonym
hypervitaminosis a (disorder)
hypervitaminosis a [disease/finding]
DOID
ICD10
UMLS
C0020579
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:8)
C0020437  |  hypercalcemia  |  2
C0022661  |  chronic kidney disease  |  1
C0027709  |  nephrocalcinosis  |  1
C0022658  |  kidney disease  |  1
C0035078  |  renal failure  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C0033845  |  pseudotumor cerebri  |  1
C0022661  |  chronic renal failure  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:62)
56603  |  CYP26B1  |  DISEASES
56993  |  TOMM22  |  DISEASES
10278  |  EFS  |  DISEASES
57167  |  SALL4  |  DISEASES
412  |  STS  |  DISEASES
1277  |  COL1A1  |  DISEASES
4256  |  MGP  |  DISEASES
6678  |  SPARC  |  DISEASES
5917  |  RARS  |  DISEASES
5947  |  RBP1  |  DISEASES
4953  |  ODC1  |  DISEASES
7276  |  TTR  |  DISEASES
27189  |  IL17C  |  DISEASES
652  |  BMP4  |  DISEASES
6662  |  SOX9  |  DISEASES
2002  |  ELK1  |  DISEASES
5914  |  RARA  |  DISEASES
10993  |  SDS  |  DISEASES
10578  |  GNLY  |  DISEASES
3589  |  IL11  |  DISEASES
1788  |  DNMT3A  |  DISEASES
5741  |  PTH  |  DISEASES
213  |  ALB  |  DISEASES
1278  |  COL1A2  |  DISEASES
51700  |  CYB5R2  |  DISEASES
1381  |  CRABP1  |  DISEASES
3479  |  IGF1  |  DISEASES
27243  |  CHMP2A  |  DISEASES
5467  |  PPARD  |  DISEASES
6578  |  SLCO2A1  |  DISEASES
8560  |  DEGS1  |  DISEASES
5551  |  PRF1  |  DISEASES
201164  |  PLD6  |  DISEASES
2314  |  FLII  |  DISEASES
7317  |  UBA1  |  DISEASES
1869  |  E2F1  |  DISEASES
6146  |  RPL22  |  DISEASES
133584  |  EGFLAM  |  DISEASES
6898  |  TAT  |  DISEASES
7323  |  UBE2D3  |  DISEASES
55503  |  TRPV6  |  DISEASES
9464  |  HAND2  |  DISEASES
57091  |  CASS4  |  DISEASES
1382  |  CRABP2  |  DISEASES
632  |  BGLAP  |  DISEASES
3713  |  IVL  |  DISEASES
4942  |  OAT  |  DISEASES
1520  |  CTSS  |  DISEASES
5950  |  RBP4  |  DISEASES
6418  |  SET  |  DISEASES
3339  |  HSPG2  |  DISEASES
650  |  BMP2  |  DISEASES
5916  |  RARG  |  DISEASES
6696  |  SPP1  |  DISEASES
7322  |  UBE2D2  |  DISEASES
387836  |  CLEC2A  |  DISEASES
117581  |  TWIST2  |  DISEASES
11331  |  PHB2  |  DISEASES
246744  |  STH  |  DISEASES
6999  |  TDO2  |  DISEASES
8972  |  MGAM  |  DISEASES
11201  |  POLI  |  DISEASES
Locus(Waiting for update.)
Disease ID 1565
Disease hypervitaminosis a
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:7)
Disease ID 1565
Disease hypervitaminosis a
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:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020579phenytoinD01067257-41-0hypervitaminosis aMESH:D006986therapeutic946392
C0020579vitamin aD01480111103-57-4hypervitaminosis aMESH:D006986marker/mechanism11824142
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)