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Pediatric Disease Annotations & Medicines



   hyperphosphatemia
  

Disease ID 1112
Disease hyperphosphatemia
Definition
A condition of abnormally high level of PHOSPHATES in the blood, usually significantly above the normal range of 0.84-1.58 mmol per liter of serum.
Synonym
hyperphosphataemia
hyperphosphatemia (disorder)
hyperphosphatemia [disease/finding]
hyperphosphatemias
DOID
UMLS
C0085681
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:29)
C0022661  |  chronic kidney disease  |  30
C0022658  |  kidney disease  |  28
C1561644  |  chronic kidney disease (ckd)  |  12
C0022661  |  end-stage renal disease  |  12
C0035078  |  renal failure  |  11
C0022658  |  renal disease  |  8
C0020502  |  hyperparathyroidism  |  6
C0022661  |  chronic renal failure  |  5
C0020503  |  secondary hyperparathyroidism  |  4
C0042373  |  vascular disease  |  4
C0007222  |  cardiovascular disease  |  3
C0033687  |  proteinuria  |  3
C0006663  |  calcinosis  |  2
C0042870  |  vitamin d defic  |  1
C0011847  |  diabetes  |  1
C0022661  |  end-stage kidney disease  |  1
C0023895  |  liver disease  |  1
C0022658  |  nephropathy  |  1
C0020492  |  hyperostosis  |  1
C0020437  |  hypercalcemia  |  1
C0020550  |  hyperthyroidism  |  1
C0002871  |  anemia  |  1
C0042870  |  vitamin d deficiency  |  1
C0006666  |  calciphylaxis  |  1
C0011849  |  diabetes mellitus  |  1
C0598608  |  hyperhomocysteinemia  |  1
C0345244  |  neuronal intestinal dysplasia  |  1
C0002895  |  sickle cell disease  |  1
C0035078  |  kidney failure  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:4)
GALNT3  |  2591  |  CTD_human
KL  |  9365  |  CTD_human
PTH  |  5741  |  CTD_human
FGF23  |  8074  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:124)
2767  |  GNA11  |  DISEASES
55808  |  ST6GALNAC1  |  DISEASES
6561  |  SLC13A1  |  DISEASES
57026  |  PDXP  |  DISEASES
1591  |  CYP24A1  |  DISEASES
3381  |  IBSP  |  DISEASES
1594  |  CYP27B1  |  DISEASES
4256  |  MGP  |  DISEASES
8074  |  FGF23  |  DISEASES
5507  |  PPP1R3C  |  DISEASES
4488  |  MSX2  |  DISEASES
6568  |  SLC17A1  |  DISEASES
3630  |  INS  |  DISEASES
26290  |  GALNT8  |  DISEASES
2056  |  EPO  |  DISEASES
10343  |  PKDREJ  |  DISEASES
1401  |  CRP  |  DISEASES
64328  |  XPO4  |  DISEASES
284904  |  SEC14L4  |  DISEASES
2012  |  EMP1  |  DISEASES
4069  |  LYZ  |  DISEASES
2201  |  FBN2  |  DISEASES
2769  |  GNA15  |  DISEASES
23476  |  BRD4  |  DISEASES
2888  |  GRB14  |  DISEASES
3938  |  LCT  |  DISEASES
6550  |  SLC9A3  |  DISEASES
8614  |  STC2  |  DISEASES
56302  |  TRPV5  |  DISEASES
127  |  ADH4  |  DISEASES
2252  |  FGF7  |  DISEASES
5045  |  FURIN  |  DISEASES
5972  |  REN  |  DISEASES
6574  |  SLC20A1  |  DISEASES
57689  |  LRRC4C  |  DISEASES
6876  |  TAGLN  |  DISEASES
4249  |  MGAT5  |  DISEASES
5741  |  PTH  |  DISEASES
56934  |  CA10  |  DISEASES
4681  |  NBL1  |  DISEASES
6781  |  STC1  |  DISEASES
1636  |  ACE  |  DISEASES
55585  |  UBE2Q1  |  DISEASES
248  |  ALPI  |  DISEASES
213  |  ALB  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
50964  |  SOST  |  DISEASES
337876  |  CHSY3  |  DISEASES
3479  |  IGF1  |  DISEASES
121340  |  SP7  |  DISEASES
10736  |  SIX2  |  DISEASES
125  |  ADH1B  |  DISEASES
79660  |  PPP1R3B  |  DISEASES
222545  |  GPRC6A  |  DISEASES
763  |  CA5A  |  DISEASES
163  |  AP2B1  |  DISEASES
6569  |  SLC34A1  |  DISEASES
5745  |  PTH1R  |  DISEASES
55432  |  YOD1  |  DISEASES
9735  |  KNTC1  |  DISEASES
1946  |  EFNA5  |  DISEASES
796  |  CALCA  |  DISEASES
2621  |  GAS6  |  DISEASES
27445  |  PCLO  |  DISEASES
8926  |  SNURF  |  DISEASES
92140  |  MTDH  |  DISEASES
6575  |  SLC20A2  |  DISEASES
1758  |  DMP1  |  DISEASES
4306  |  NR3C2  |  DISEASES
54914  |  FOCAD  |  DISEASES
51460  |  SFMBT1  |  DISEASES
55503  |  TRPV6  |  DISEASES
4151  |  MB  |  DISEASES
11169  |  WDHD1  |  DISEASES
140803  |  TRPM6  |  DISEASES
56955  |  MEPE  |  DISEASES
56259  |  CTNNBL1  |  DISEASES
142680  |  SLC34A3  |  DISEASES
2590  |  GALNT2  |  DISEASES
6708  |  SPTA1  |  DISEASES
632  |  BGLAP  |  DISEASES
148534  |  TMEM56  |  DISEASES
164045  |  HFM1  |  DISEASES
2258  |  FGF13  |  DISEASES
2778  |  GNAS  |  DISEASES
8675  |  STX16  |  DISEASES
860  |  RUNX2  |  DISEASES
26301  |  GBGT1  |  DISEASES
310  |  ANXA7  |  DISEASES
5464  |  PPA1  |  DISEASES
249  |  ALPL  |  DISEASES
79695  |  GALNT12  |  DISEASES
63940  |  GPSM3  |  DISEASES
8859  |  STK19  |  DISEASES
6392  |  SDHD  |  DISEASES
1471  |  CST3  |  DISEASES
54897  |  CASZ1  |  DISEASES
650  |  BMP2  |  DISEASES
5251  |  PHEX  |  DISEASES
9247  |  GCM2  |  DISEASES
79625  |  NDNF  |  DISEASES
54809  |  SAMD9  |  DISEASES
9365  |  KL  |  DISEASES
10568  |  SLC34A2  |  DISEASES
250  |  ALPP  |  DISEASES
2591  |  GALNT3  |  DISEASES
114805  |  GALNT13  |  DISEASES
6696  |  SPP1  |  DISEASES
655  |  BMP7  |  DISEASES
5744  |  PTHLH  |  DISEASES
7018  |  TF  |  DISEASES
10636  |  RGS14  |  DISEASES
2260  |  FGFR1  |  DISEASES
197  |  AHSG  |  DISEASES
6424  |  SFRP4  |  DISEASES
846  |  CASR  |  DISEASES
57451  |  TENM2  |  DISEASES
7421  |  VDR  |  DISEASES
8972  |  MGAM  |  DISEASES
567  |  B2M  |  DISEASES
246734  |  NPCDR1  |  DISEASES
149775  |  GNAS-AS1  |  DISEASES
102723508  |  KANTR  |  DISEASES
103164619  |  PCAT2  |  DISEASES
Locus(Waiting for update.)
Disease ID 1112
Disease hyperphosphatemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:27)
HP:0012622  |  Chronic kidney disease  |  30
HP:0003774  |  End-stage renal failure  |  17
HP:0000083  |  Renal insufficiency  |  11
HP:0004934  |  Vascular calcification  |  11
HP:0002901  |  Hypocalcemia  |  7
HP:0000843  |  Hyperparathyroidism  |  5
HP:0000867  |  Secondary hyperparathyroidism  |  3
HP:0000093  |  Proteinuria  |  3
HP:0002664  |  Neoplasia  |  3
HP:0000829  |  Hypoparathyroidism  |  2
HP:0010766  |  Ectopic calcification  |  2
HP:0003761  |  Calcinosis  |  2
HP:0001712  |  Left ventricular hypertrophy  |  1
HP:0100512  |  Vitamin D deficiency  |  1
HP:0011915  |  Cardiovascular calcification  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0100774  |  Hyperostosis  |  1
HP:0001903  |  Anemia  |  1
HP:0001714  |  Ventricular hypertrophy  |  1
HP:0000836  |  Overactive thyroid  |  1
HP:0003072  |  Hypercalcemia  |  1
HP:0002925  |  Increased serum thyroid-stimulating hormone  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0004325  |  Low body weight  |  1
HP:0000112  |  Nephropathy  |  1
HP:0002315  |  Headaches  |  1
HP:0011001  |  Increased bone mineral density  |  1
Disease ID 1112
Disease hyperphosphatemia
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0020598  |  hypocalcemia  |  7
C0006663  |  calcinosis  |  2
C0263628  |  tumoral calcinosis  |  2
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:4)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0085681calcitriolD00211732222-06-3hyperphosphatemiaMESH:D054559marker/mechanism11981061
C0085681oxytetracyclineD01011879-57-2hyperphosphatemiaMESH:D054559marker/mechanism8905581
C0085681pamidronateC01924840391-99-9hyperphosphatemiaMESH:D054559therapeutic10490077
C0085681cholecalciferolD00276267-97-0hyperphosphatemiaMESH:D054559marker/mechanism10490077
FDA approved drug and dosage information(Total Drugs:1)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D054559calcijexcalcitriol0.001MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsINJECTABLE;INJECTIONDiscontinuedNoneYesNo
FDA labeling changes(Total Drugs:1)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D05455911/16/2001calcijexcalcitriolManagement of hypocalcemia in patients undergoing chronic renal dialysisThe safety and effectiveness of calcitriol was examined in a double-blind placebo-controlled trial of 35 pediatric patients (13-18 years of age) with end-stage renal disease and on dialysis. The primary efficacy endpoint favored the calcitriol-treated versus the placebo-treated patients Transient hypercalcemia was seen in 1 of 16 calcitriol-treated patients; 6 of 16 (38%) calcitriol-treated patients and 2 of 19 (11%) placebo-treated patients had Ca x P >75LabelingB---Abbott02/16/2001FALSE'