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Pediatric Disease Annotations & Medicines



   hyperaldosteronism
  

Disease ID 442
Disease hyperaldosteronism
Definition
A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA.
Synonym
aldosteronism
aldosteronism (disorder)
aldosteronism nos
aldosteronism, nos
elevated plasma aldosterone
hyperaldosteronism [disease/finding]
hyperaldosteronism nos
hyperaldosteronism nos (disorder)
hyperaldosteronism, nos
hyperaldosteronism, unspecified
increased aldosterone
increased aldosterone production
mineralocorticoid excess
DOID
ICD10
UMLS
C0020428
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:26)
C0020538  |  hypertension  |  13
C0001430  |  adenoma  |  3
C0020502  |  hyperparathyroidism  |  2
C1621895  |  adrenal hyperplasia  |  2
C1384514  |  primary aldosteronism  |  2
C0018801  |  heart failure  |  2
C0334684  |  renal adenoma  |  1
C0001815  |  myeloid metaplasia  |  1
C0001622  |  hypercortisolism  |  1
C0027819  |  neuroblastoma  |  1
C0011847  |  diabetes  |  1
C0037315  |  sleep apnea  |  1
C0031036  |  polyarteritis nodosa  |  1
C0206667  |  adrenocortical adenoma  |  1
C0025286  |  meningioma  |  1
C0030443  |  periodic paralysis  |  1
C0221002  |  primary hyperparathyroidism  |  1
C0022658  |  kidney disease  |  1
C0022661  |  chronic kidney disease  |  1
C0027709  |  nephrocalcinosis  |  1
C0033804  |  pseudohermaphroditism  |  1
C0010481  |  cushing syndrome  |  1
C0011991  |  diarrhea  |  1
C0206667  |  adrenal adenoma  |  1
C0085580  |  essential hypertension  |  1
C0155616  |  secondary hypertension  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
ATP1A1  |  476  |  CTD_human
CACNA1D  |  776  |  CTD_human
CYP11B2  |  1585  |  CTD_human
CYP11B1  |  1584  |  CTD_human
ATP2B3  |  492  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:111)
1407  |  CRY1  |  DISEASES
2798  |  GNRHR  |  DISEASES
2908  |  NR3C1  |  DISEASES
8074  |  FGF23  |  DISEASES
65266  |  WNK4  |  DISEASES
29802  |  VPREB3  |  DISEASES
53947  |  A4GALT  |  DISEASES
3630  |  INS  |  DISEASES
50617  |  ATP6V0A4  |  DISEASES
3958  |  LGALS3  |  DISEASES
10542  |  LAMTOR5  |  DISEASES
10060  |  ABCC9  |  DISEASES
5597  |  MAPK6  |  DISEASES
54962  |  TIPIN  |  DISEASES
9252  |  RPS6KA5  |  DISEASES
6558  |  SLC12A2  |  DISEASES
23476  |  BRD4  |  DISEASES
492  |  ATP2B3  |  DISEASES
1716  |  DGUOK  |  DISEASES
5443  |  POMC  |  DISEASES
118  |  ADD1  |  DISEASES
8622  |  PDE8B  |  DISEASES
6550  |  SLC9A3  |  DISEASES
3827  |  KNG1  |  DISEASES
9746  |  CLSTN3  |  DISEASES
1583  |  CYP11A1  |  DISEASES
79798  |  ARMC5  |  DISEASES
5972  |  REN  |  DISEASES
805  |  CALM2  |  DISEASES
185  |  AGTR1  |  DISEASES
3779  |  KCNMB1  |  DISEASES
2768  |  GNA12  |  DISEASES
57786  |  RBAK  |  DISEASES
6770  |  STAR  |  DISEASES
1392  |  CRH  |  DISEASES
5741  |  PTH  |  DISEASES
23250  |  ATP11A  |  DISEASES
50940  |  PDE11A  |  DISEASES
9073  |  CLDN8  |  DISEASES
776  |  CACNA1D  |  DISEASES
22808  |  MRAS  |  DISEASES
1636  |  ACE  |  DISEASES
808  |  CALM3  |  DISEASES
1584  |  CYP11B1  |  DISEASES
162417  |  NAGS  |  DISEASES
3973  |  LHCGR  |  DISEASES
476  |  ATP1A1  |  DISEASES
213  |  ALB  |  DISEASES
552  |  AVPR1A  |  DISEASES
6340  |  SCNN1G  |  DISEASES
55872  |  PBK  |  DISEASES
5617  |  PRL  |  DISEASES
51305  |  KCNK9  |  DISEASES
255738  |  PCSK9  |  DISEASES
10736  |  SIX2  |  DISEASES
3777  |  KCNK3  |  DISEASES
7369  |  UMOD  |  DISEASES
7201  |  TRHR  |  DISEASES
10008  |  KCNE3  |  DISEASES
65125  |  WNK1  |  DISEASES
3291  |  HSD11B2  |  DISEASES
8630  |  HSD17B6  |  DISEASES
54822  |  TRPM7  |  DISEASES
1555  |  CYP2B6  |  DISEASES
55553  |  SOX6  |  DISEASES
1585  |  CYP11B2  |  DISEASES
9622  |  KLK4  |  DISEASES
5121  |  PCP4  |  DISEASES
4158  |  MC2R  |  DISEASES
8912  |  CACNA1H  |  DISEASES
153571  |  C5orf38  |  DISEASES
93974  |  ATPIF1  |  DISEASES
4221  |  MEN1  |  DISEASES
3753  |  KCNE1  |  DISEASES
3762  |  KCNJ5  |  DISEASES
4306  |  NR3C2  |  DISEASES
54681  |  P4HTM  |  DISEASES
4929  |  NR4A2  |  DISEASES
6338  |  SCNN1B  |  DISEASES
1811  |  SLC26A3  |  DISEASES
200734  |  SPRED2  |  DISEASES
801  |  CALM1  |  DISEASES
5573  |  PRKAR1A  |  DISEASES
6337  |  SCNN1A  |  DISEASES
5575  |  PRKAR1B  |  DISEASES
3164  |  NR4A1  |  DISEASES
3360  |  HTR4  |  DISEASES
183  |  AGT  |  DISEASES
6446  |  SGK1  |  DISEASES
480  |  ATP1A4  |  DISEASES
3283  |  HSD3B1  |  DISEASES
3284  |  HSD3B2  |  DISEASES
1586  |  CYP17A1  |  DISEASES
7809  |  BSND  |  DISEASES
774  |  CACNA1B  |  DISEASES
2516  |  NR5A1  |  DISEASES
249  |  ALPL  |  DISEASES
1188  |  CLCNKB  |  DISEASES
4878  |  NPPA  |  DISEASES
9365  |  KL  |  DISEASES
551  |  AVP  |  DISEASES
6557  |  SLC12A1  |  DISEASES
50834  |  TAS2R1  |  DISEASES
3758  |  KCNJ1  |  DISEASES
3778  |  KCNMA1  |  DISEASES
6559  |  SLC12A3  |  DISEASES
1408  |  CRY2  |  DISEASES
408  |  ARRB1  |  DISEASES
8972  |  MGAM  |  DISEASES
2232  |  FDXR  |  DISEASES
285943  |  HOXA-AS2  |  DISEASES
Locus(Waiting for update.)
Disease ID 442
Disease hyperaldosteronism
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:31)
HP:0000822  |  Hypertension  |  13
HP:0200114  |  Metabolic alkalosis  |  4
HP:0001948  |  Alkalosis  |  4
HP:0002900  |  Hypokalemia  |  4
HP:0002615  |  Low blood pressure  |  3
HP:0001960  |  Hypokalemic metabolic alkalosis  |  2
HP:0003470  |  Inability to move  |  2
HP:0008221  |  Enlarged adrenal glands  |  2
HP:0000843  |  Hyperparathyroidism  |  2
HP:0001578  |  Hypercortisolism  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0000848  |  Hyperreninemia  |  2
HP:0011675  |  Arrhythmias  |  1
HP:0002014  |  Diarrhea  |  1
HP:0001685  |  Myocardial fibrosis  |  1
HP:0003768  |  Periodic paralysis  |  1
HP:0002385  |  Paraparesis  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0002104  |  Absence of spontaneous respiration  |  1
HP:0012622  |  Chronic kidney disease  |  1
HP:0002917  |  Low blood magnesium levels  |  1
HP:0002858  |  Mengiomia  |  1
HP:0004308  |  Ventricular arrhythmia  |  1
HP:0002150  |  Hypercalcinuria  |  1
HP:0008256  |  Adrenocortical adenomas  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0000037  |  Male pseudohermaphroditism  |  1
HP:0012408  |  Medullary nephrocalcinosis  |  1
HP:0008200  |  Primary hyperparathyroidism  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0000121  |  Nephrocalcinosis  |  1
Disease ID 442
Disease hyperaldosteronism
Manually Symptom
UMLS  | Name(Total Manually Symptoms:15)
C2364118  |  weakness
C1963138  |  hypertension
C1609519  |  adrenal myelolipoma
C1555754  |  cardiovascular disease
C1279412  |  periodic paralysis syndrome
C0334684  |  renal adenoma
C0232197  |  fibrillation
C0220983  |  metabolic alkalosis
C0206635  |  myelolipoma
C0162565  |  acute intermittent porphyria
C0033806  |  pseudohypoparathyroidism
C0020538  |  vascular hypertension
C0020488  |  sodium retention
C0010481  |  hypercortisolism
C0003125  |  anorexia nervosa
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:6)
C0020538  |  hypertension  |  13
C0220983  |  metabolic alkalosis  |  4
C0001622  |  hypercortisolism  |  1
C0020488  |  sodium retention  |  1
C0206635  |  myelolipoma  |  1
C0334684  |  renal adenoma  |  1
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:6)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020428bendroflumethiazideD00153973-48-3hyperaldosteronismMESH:D006929therapeutic20009770
C0020428capreomycinD00220711003-38-6hyperaldosteronismMESH:D006929marker/mechanism5489186
C0020428chlorthalidoneD00275277-36-1hyperaldosteronismMESH:D006929marker/mechanism1103606
C0020428spironolactoneD0131481952/1/7hyperaldosteronismMESH:D006929marker/mechanism1103606
C0020428spironolactoneD0131481952/1/7hyperaldosteronismMESH:D006929therapeutic19224505
C0020428streptozocinD01331118883-66-4hyperaldosteronismMESH:D006929marker/mechanism2819817
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)