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Details
Link-It Detail - Human Phenotype - Abnormality of renal excretion
Debug Stats
  • ### Total Build Time: 32 ms 29.375 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 205 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 452 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.048 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 2.100 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 23.193 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of renal excretion HP:0011036
Definition (1)
An altered ability of the kidneys to void urine and/or specific substances.
Parents (1)
img Abnormality of renal physiology HP:0000082
Children (6)
img Polyuria HP:0000103
img Impaired renal uric acid clearance HP:0004732
img Decreased urine output HP:0011037
img Increased urine output HP:0200060
img Reduced creatinine clearance HP:0000120
img Decreased renal tubular phosphate excretion HP:0005572
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of renal physiology HP:0000082
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of renal physiology HP:0000082
Genes (49)

Species:
human : 49
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNPHP4261734nephronophthisis 4
img HP RolledUp, OMIM ID: 606996
img HP RolledUp, OMIM ID: 606966
HumanSLSN3260432Senior-Loken syndrome 3
img HP RolledUp, OMIM ID: 606995
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 613550
HumanSARS254938seryl-tRNA synthetase 2, mitochondrial
img HP RolledUp, OMIM ID: 613845
HumanFOXP350943forkhead box P3
img HP RolledUp, OMIM ID: 222100
HumanNPHP327031nephronophthisis 3 (adolescent)
img HP RolledUp, OMIM ID: 604387
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img HP RolledUp, OMIM ID: 222100
HumanCFHR310878complement factor H-related 3
img HP RolledUp, OMIM ID: 235400
HumanCLDN1610686claudin 16
img HP RolledUp, OMIM ID: 248250
HumanSH2B310019SH2B adaptor protein 3
img HP RolledUp, OMIM ID: 222100
HumanKL9365klotho
img HP RolledUp, OMIM ID: 211900
HumanFGF238074fibroblast growth factor 23
img HP RolledUp, OMIM ID: 211900
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img HP RolledUp, OMIM ID: 602522
HumanTHBD7056thrombomodulin
img HP RolledUp, OMIM ID: 612926
HumanHNF1A6927HNF1 homeobox A
img HP RolledUp, OMIM ID: 222100
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img HP RolledUp, OMIM ID: 263800
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img HP RolledUp, OMIM ID: 601678
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
img HP RolledUp, OMIM ID: 233100
HumanREN5972renin
img HP RolledUp, OMIM ID: 267430
HumanOAS149382'-5'-oligoadenylate synthetase 1, 40/46kDa
img HP RolledUp, OMIM ID: 222100
HumanNPHP14867nephronophthisis 1 (juvenile)
img HP RolledUp, OMIM ID: 266900
img HP RolledUp, OMIM ID: 256100
HumanMUC14582mucin 1, cell surface associated
img HP RolledUp, OMIM ID: 174000
HumanCD464179CD46 molecule, complement regulatory protein
img HP RolledUp, OMIM ID: 612922
img HP RolledUp, OMIM ID: 235400
HumanMCKD14169medullary cystic kidney disease 1 (autosomal dominant)
img HP RolledUp, OMIM ID: 174000
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
img HP RolledUp, OMIM ID: 612780
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011036Abnormality of renal excretion0self