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Details
Link-It Detail - Disease - Hypoaldosteronism
Debug Stats
  • ### Total Build Time: 38 ms 13.304 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 464 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 557 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=11 ms Completed: 11 ms rowSize= 4.579 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 4.518 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypoaldosteronism C0020595
Definition (1)
A congenital or acquired condition of insufficient production of ALDOSTERONE by the ADRENAL CORTEX leading to diminished aldosterone-mediated synthesis of Na(+)-K(+)-EXCHANGING ATPASE in renal tubular cells. Clinical symptoms include HYPERKALEMIA, sodium-wasting, HYPOTENSION, and sometimes metabolic ACIDOSIS.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Adrenal Insufficiency C0001623
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Adrenal Gland Diseases C00016214img Adrenal Insufficiency C0001623
Relationships (9)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 7
diso_​to_​phen : 1


Relationships:
none : 6
isa : 2
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO11img Complication Aspects C1171258
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_DISO7img Hyperkalemia C0020461
DISO_to_DISO6img Hyperkalemia C0020461
DISO_to_PHEN6img genetic aspects C0017399
DISO_to_ANAT5img In Blood C0005768
DISO_to_DISOmapped_toimg Corticosterone Methyl Oxidase Type I Deficiency C0268293
DISO_to_DISOisaimg Hyperreninemic hypoaldosteronism C0342483
DISO_to_DISOisaimg Hypoaldosteronism, Hyporeninemic C0376185
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
img OMIM, Score=1000, UMLKSK CUI: C0020595
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0020595
HumanCYP11B21585cytochrome P450, family 11, subfamily B, polypeptide 2
img GENERIF, Score=913, Pubmed Id: 15699546, UMLKSK CUI: C0020595
img OMIM, Score=1000, UMLKSK CUI: C0020595
HumanAIRE326autoimmune regulator
img OMIM, Score=1000, UMLKSK CUI: C0020595
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020595Hypoaldosteronism0self