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Details
Link-It Detail - Human Phenotype - Abnormality of aldosterone production
Debug Stats
  • ### Total Build Time: 24 ms 26.906 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 761 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.090 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.090 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of aldosterone production HP:0002855
Namespace (1)
medical_genetics
Parents (1)
img Adrenocortical abnormality HP:0000849
Children (2)
img Hyperaldosteronism HP:0000859
img Hypoaldosteronism HP:0004319
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Adrenocortical abnormality HP:0000849
img All HP:0000001img Phenotypic abnormality HP:00001187img Adrenocortical abnormality HP:0000849
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanLHX489884LIM homeobox 4
img HP RolledUp, OMIM ID: 262700
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
img HP RolledUp, OMIM ID: 231550
HumanLHX38022LIM homeobox 3
img HP RolledUp, OMIM ID: 262600
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img HP RolledUp, OMIM ID: 602522
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img HP RolledUp, OMIM ID: 601678
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
img HP RolledUp, OMIM ID: 264350
img HP RolledUp, OMIM ID: 177200
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
img HP RolledUp, OMIM ID: 264350
img HP RolledUp, OMIM ID: 177200
HumanSCNN1A6337sodium channel, non-voltage-gated 1 alpha subunit
img HP RolledUp, OMIM ID: 264350
HumanPROP15626PROP paired-like homeobox 1
img HP RolledUp, OMIM ID: 262600
HumanPOU1F15449POU class 1 homeobox 1
img HP RolledUp, OMIM ID: 262600
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img HP RolledUp, OMIM ID: 309000
HumanNR3C24306nuclear receptor subfamily 3, group C, member 2
img HP RolledUp, OMIM ID: 177735
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
img HP RolledUp, OMIM ID: 612780
HumanKCNJ53762potassium inwardly-rectifying channel, subfamily J, member 5
img HP RolledUp, OMIM ID: 613677
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img HP RolledUp, OMIM ID: 241200
HumanHSD11B23291hydroxysteroid (11-beta) dehydrogenase 2
img HP RolledUp, OMIM ID: 218030
HumanSLC26A31811solute carrier family 26 (anion exchanger), member 3
img HP RolledUp, OMIM ID: 214700
HumanCYP11B21585cytochrome P450, family 11, subfamily B, polypeptide 2
img HP RolledUp, OMIM ID: 124080
img HP RolledUp, OMIM ID: 610600
img HP RolledUp, OMIM ID: 203400
HumanCYP11B11584cytochrome P450, family 11, subfamily B, polypeptide 1
img HP RolledUp, OMIM ID: 103900
HumanCYP11A11583cytochrome P450, family 11, subfamily A, polypeptide 1
img HP RolledUp, OMIM ID: 613743
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img HP RolledUp, OMIM ID: 613090
img HP RolledUp, OMIM ID: 607364
img HP RolledUp, OMIM ID: 602522
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img HP RolledUp, OMIM ID: 602522
img HP RolledUp, OMIM ID: 613090
HumanAIRE326autoimmune regulator
img HP RolledUp, OMIM ID: 240300
HumanNR0B1190nuclear receptor subfamily 0, group B, member 1
img HP RolledUp, OMIM ID: 300200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002855Abnormality of aldosterone production0self