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Details
Link-It Detail - Human Phenotype - Abnormality of the kidney
Debug Stats
  • ### Total Build Time: 84 ms 43.607 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 196 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= 795 bytes
  • CONCEPT_CHILDREN gt=14 ms Completed: 14 ms rowSize= 15.404 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.108 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=56 ms Completed: 56 ms rowSize= 23.768 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the kidney HP:0000077
Definition (1)
An abnormality of the `kidney` (FMA:7203).
Parents (2)
img Abnormality of the urinary system HP:0000079
img Abnormality of the upper urinary tract HP:0010935
Children (48)
img Abnormality of the renal tubule HP:0000091
img Renal amyloidosis HP:0001917
img Abnormal renal corticomedullary differentiation HP:0005932
img Nephronophthisis HP:0000090
img Hematuria HP:0000790
img Kidney malformation HP:0000792
img Enlarged kidneys HP:0000105
img Hydronephrosis HP:0000126
img Renal hamartoma HP:0008696
img Renal neoplasm HP:0009726
img Nephrogenic rest HP:0100880
img Renal duplication HP:0000075
img Abnormality of the renal collecting system HP:0004742
img Renal hypoplasia/aplasia HP:0008678
img Renal dysplasia HP:0000110
img Orotic acid urinary obstruction HP:0000810
img Ectopic kidney HP:0000086
img Renal agenesis HP:0000104
img Renal malrotation HP:0004712
img Structural anomalies of the renal tract HP:0004735
img Hemolytic-uremic syndrome HP:0005575
img Horseshoe kidney HP:0000085
img Nephropathy HP:0000112
img Mesangial abnormality HP:0001966
img Renal cortical atrophy HP:0002048
img Abnormal renal physiology HP:0012211
img Elevated alkaline phosphatase of renal origin HP:0010680
img Abnormality of the renal cortex HP:0011035
img Abnormal renal morphology HP:0012210
img Fatty kidney HP:0000799
img Morphological abnormalities of the glomeruli HP:0000095
img Nephrosis HP:0000801
img Nephrocalcinosis HP:0000121
img Megacalicosis HP:0100581
img Unilateral renal atrophy HP:0008717
img Abnormality of the renal medulla HP:0100957
img Lobular glomerulopathy HP:0008636
img Renal cysts HP:0000107
img Abnormality of renal physiology HP:0000082
img Nephritis HP:0000123
img Nephrolithiasis HP:0000787
img Low alkaline phosphatase of renal origin HP:0010685
img Glomerulopathy HP:0100820
img Abnormality of the renal artery HP:0008776
img Abnormality of the renal pelvis HP:0010944
img Nephrosclerosis HP:0009741
img Abnormality of renal calyx morphology HP:0011130
img Abnormal localization of kidneys HP:0100542
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the urinary system HP:0000079
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the upper urinary tract HP:0010935
Genes (706)

Species:
human : 706
Page Size
Current 25
  Page 1 of 29
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanHNFJ3100689490Hyperuricemic nephropathy, familial juvenile, 3
img HP RolledUp, OMIM ID: 614227
HumanGFND1100689213Glomerulopathy with fibronectin deposits 1
img HP RolledUp, OMIM ID: 137950
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanIGAN2100653384IgA nephropathy, susceptibility to, 2
img HP RolledUp, OMIM ID: 613944
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL11P13100528024Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
img HP RolledUp, OMIM ID: 194072
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP PCS, OMIM ID: 607872
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
img HP RolledUp, OMIM ID: 612089
HumanIH100188864Hemihypertrophy
img HP RolledUp, OMIM ID: 235000
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP PCS, OMIM ID: 610543
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img HP RolledUp, OMIM ID: 152700
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanDIP100188011interstitial pneumonitis, desquamative, familial
img HP RolledUp, OMIM ID: 263000
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000077Abnormality of the kidney0self