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Details
Link-It Detail - Human Phenotype - Abnormal circulating creatinine level
Debug Stats
  • ### Total Build Time: 13 ms 18.477 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 236 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=0 Completed: 0 ms rowSize= 465 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 777 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.180 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 14.471 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal circulating creatinine level HP:0012100
Definition (1)
An abnormal concentration of `creatinine` (CHEBI:16737) in the `blood` (FMA:9670).
Parents (1)
img Abnormality of nitrogen compound homeostasis HP:0004364
Children (2)
img Decreased serum creatinine HP:0012101
img Elevated serum creatinine HP:0003259
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of nitrogen compound homeostasis HP:0004364
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanRFH159331Renal failure, progressive, with hypertension
img HP RolledUp, OMIM ID: 161900
HumanWDR1957728WD repeat domain 19
img HP RolledUp, OMIM ID: 614376
HumanINVS27130inversin
img HP RolledUp, OMIM ID: 602088
HumanFAN122909FANCD2/FANCI-associated nuclease 1
img HP RolledUp, OMIM ID: 614817
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
img HP RolledUp, OMIM ID: 274150
HumanCFHR310878complement factor H-related 3
img HP RolledUp, OMIM ID: 235400
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
img HP RolledUp, OMIM ID: 223900
HumanTHBD7056thrombomodulin
img HP RolledUp, OMIM ID: 612926
HumanHNF1B6928HNF1 homeobox B
img HP RolledUp, OMIM ID: 137920
HumanMUC14582mucin 1, cell surface associated
img HP RolledUp, OMIM ID: 174000
HumanCD464179CD46 molecule, complement regulatory protein
img HP RolledUp, OMIM ID: 235400
img HP RolledUp, OMIM ID: 612922
HumanMCKD14169medullary cystic kidney disease 1 (autosomal dominant)
img HP RolledUp, OMIM ID: 174000
HumanCFI3426complement factor I
img HP RolledUp, OMIM ID: 612923
img HP RolledUp, OMIM ID: 235400
HumanCFHR13078complement factor H-related 1
img HP RolledUp, OMIM ID: 235400
HumanCFH3075complement factor H
img HP RolledUp, OMIM ID: 235400
HumanC3718complement component 3
img HP RolledUp, OMIM ID: 612925
HumanCFB629complement factor B
img HP RolledUp, OMIM ID: 612924
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012100Abnormal circulating creatinine level0self