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Details
Link-It Detail - Human Phenotype - Abnormal albumin level
Debug Stats
  • ### Total Build Time: 65 ms 22.306 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 197 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 244 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=28 ms Completed: 28 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 461 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 757 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 18.349 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal albumin level HP:0012116
Definition (1)
Deviation from normal concentration of `albumin` (PR:000003918) in the `blood` (FMA:9670).
Parents (1)
img Abnormality of circulating protein level HP:0010876
Children (2)
img Hypoalbuminemia HP:0003073
img Hyperalbuminemia HP:0012117
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of circulating protein level HP:0010876
Genes (23)

Species:
human : 23
SpeciesGeneGeneIdGene NameEvidence
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanC10orf256652chromosome 10 open reading frame 2
img HP RolledUp, OMIM ID: 251880
HumanAPTX54840aprataxin
img HP RolledUp, OMIM ID: 208920
HumanPLCE151196phospholipase C, epsilon 1
img HP RolledUp, OMIM ID: 610725
HumanSAR1B51128SAR1 homolog B (S. cerevisiae)
img HP RolledUp, OMIM ID: 246700
HumanHPLH127259hemophagocytic lymphohistiocytosis 1
img HP RolledUp, OMIM ID: 267700
HumanTTC379652tetratricopeptide repeat domain 37
img HP RolledUp, OMIM ID: 222470
HumanSUCLA28803succinate-CoA ligase, ADP-forming, beta subunit
img HP RolledUp, OMIM ID: 251880
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
img HP RolledUp, OMIM ID: 600995
HumanTK27084thymidine kinase 2, mitochondrial
img HP RolledUp, OMIM ID: 251880
HumanPTPRO5800protein tyrosine phosphatase, receptor type, O
img HP RolledUp, OMIM ID: 614196
HumanPTEN5728phosphatase and tensin homolog
img HP RolledUp, OMIM ID: 174900
HumanPRF15551perforin 1 (pore forming protein)
img HP RolledUp, OMIM ID: 603553
HumanPMM25373phosphomannomutase 2
img HP RolledUp, OMIM ID: 212065
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
img HP RolledUp, OMIM ID: 256300
HumanMYO1E4643myosin IE
img HP RolledUp, OMIM ID: 614131
HumanMPV174358MpV17 mitochondrial inner membrane protein
img HP RolledUp, OMIM ID: 251880
HumanMPI4351mannose phosphate isomerase
img HP RolledUp, OMIM ID: 602579
HumanSMAD44089SMAD family member 4
img HP RolledUp, OMIM ID: 174900
HumanDGUOK1716deoxyguanosine kinase
img HP RolledUp, OMIM ID: 251880
HumanBMPR1A657bone morphogenetic protein receptor, type IA
img HP RolledUp, OMIM ID: 174900
HumanB2M567beta-2-microglobulin
img HP RolledUp, OMIM ID: 241600
HumanACTN481actinin, alpha 4
img HP RolledUp, OMIM ID: 603278
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012116Abnormal albumin level0self