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Details
Link-It Detail - Disease - Hyperaldosteronism
Debug Stats
  • ### Total Build Time: 202 ms 28.652 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 319 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 554 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 1.522 KB
  • CONCEPT_RELATIONSHIPS gt=127 ms Completed: 127 ms rowSize= 12.895 KB
  • CONCEPT_GENES gt=33 ms Completed: 33 ms rowSize= 11.143 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperaldosteronism C0020428
Definition (1)
A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Adrenocortical Hyperfunction C0001622
Children (1)
img Bartter Syndrome C0004775
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Adrenal Gland Diseases C00016214img Adrenocortical Hyperfunction C0001622
Relationships (47)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 13
diso_​to_​diso : 27
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 31
classifies : 1
isa : 4
mapped_​to : 5
may_​treat : 5
use : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO198img Complication Aspects C1171258
DISO_to_DISO168img Hypertension C0020538
DISO_to_DISO144img Complication Aspects C1171258
DISO_to_ANAT131img In Blood C0005768
DISO_to_DISO116img Hypertension C0020538
DISO_to_CHEM114img Aldosterone C0002006
DISO_to_ANAT88img In Blood C0005768
DISO_to_CHEM78img Aldosterone C0002006
DISO_to_PHEN75img genetic aspects C0017399
DISO_to_ANAT63img Adrenal Glands C0001625
DISO_to_DISO59img Adrenal Gland Neoplasms C0001624
DISO_to_DISO50img Adenoma C0001430
DISO_to_DISO49img Adrenal Cortex Neoplasms C0001618
DISO_to_DISO46img Adrenal Gland Neoplasms C0001624
DISO_to_DISO44img Adrenocortical Adenoma C0206667
DISO_to_CHEM38img Renin C0035094
DISO_to_DISO33img Adenoma C0001430
DISO_to_PHEN33img genetic aspects C0017399
DISO_to_CHEM32img Renin C0035094
DISO_to_CHEM27img Mineralocorticoid Receptor Antagonists C1579268
DISO_to_DISO24img Adrenal Cortical Adenoma C0206667
DISO_to_DISO22img Adrenal Cortex Neoplasms C0001618
DISO_to_DISO22img Hypokalemia C0020621
DISO_to_ANAT21img Adrenal Glands C0001625
DISO_to_CHEM21img Hydrocortisone C0020268
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img OMIM, Score=1000, UMLKSK CUI: C0020428
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanRGS25997regulator of G-protein signaling 2, 24kDa
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanMEN14221multiple endocrine neoplasia I
img GENERIF, Score=861, Pubmed Id: 11903322, UMLKSK CUI: C0020428
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanCYP17A11586cytochrome P450, family 17, subfamily A, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0020428
HumanCYP11B21585cytochrome P450, family 11, subfamily B, polypeptide 2
img GENERIF, Score=861, Pubmed Id: 11903322, UMLKSK CUI: C0020428
HumanCYP11B11584cytochrome P450, family 11, subfamily B, polypeptide 1
img GENERIF, Score=861, Pubmed Id: 11903322, UMLKSK CUI: C0020428
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img OMIM, Score=1000, UMLKSK CUI: C0020428
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img OMIM, Score=1000, UMLKSK CUI: C0020428
HumanAGTR1185angiotensin II receptor, type 1
img GENERIF, Score=861, Pubmed Id: 11903322, UMLKSK CUI: C0020428
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020428Hyperaldosteronism0self