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Details
Link-It Detail - Human Phenotype - Abnormality of fluid regulation
Debug Stats
  • ### Total Build Time: 238 ms 26.797 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 217 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=6 ms Completed: 6 ms rowSize= 458 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 742 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.173 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=226 ms Completed: 226 ms rowSize= 22.869 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of fluid regulation HP:0011032
Definition (1)
An abnormality of the `regulation of body fluids` (GO:0050878).
Parents (1)
img Abnormality of metabolism/homeostasis HP:0001939
Children (2)
img Edema HP:0000969
img Dehydration HP:0001944
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
Genes (263)

Species:
human : 263
Page Size
Current 25
  Page 1 of 11
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanLMPH1B100188865Lymphedema, hereditary, IB
img HP RolledUp, OMIM ID: 611944
HumanFECD2100188278corneal dystrophy, Fuchs endothelial 2
img HP RolledUp, OMIM ID: 610158
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 604131
HumanZFP57346171ZFP57 zinc finger protein
img HP RolledUp, OMIM ID: 601410
HumanMMS338340Malignant mesothelioma, susceptibility to
img HP RolledUp, OMIM ID: 156240
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img HP RolledUp, OMIM ID: 251110
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanCMAL246230Capillary malformations, hereditary
img HP RolledUp, OMIM ID: 163000
HumanHEPACAM220296hepatic and glial cell adhesion molecule
img HP RolledUp, OMIM ID: 604004
HumanSTOX1219736storkhead box 1
img HP RolledUp, OMIM ID: 189800
HumanACSF3197322acyl-CoA synthetase family member 3
img HP RolledUp, OMIM ID: 614265
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
img HP RolledUp, OMIM ID: 251100
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanCDAN1146059codanin 1
img HP RolledUp, OMIM ID: 224120
HumanDIS3L2129563DIS3 mitotic control homolog (S. cerevisiae)-like 2
img HP RolledUp, OMIM ID: 267000
HumanNDUFA11126328NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa
img HP RolledUp, OMIM ID: 252010
HumanANTXR2118429anthrax toxin receptor 2
img HP RolledUp, OMIM ID: 236490
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 120100
img HP RolledUp, OMIM ID: 607115
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img HP RolledUp, OMIM ID: 252010
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011032Abnormality of fluid regulation0self