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Details
Link-It Detail - Human Phenotype - Abnormal renal morphology
Debug Stats
  • ### Total Build Time: 50 ms 29.801 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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= 446 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 8.109 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 2.088 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 17.609 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal renal morphology HP:0012210
Definition (1)
Any structural anomaly of the `kidney` (FMA:7203).
Parents (1)
img Abnormality of the kidney HP:0000077
Children (25)
img Abnormality of the renal tubule HP:0000091
img Renal amyloidosis HP:0001917
img Kidney malformation HP:0000792
img Enlarged kidneys HP:0000105
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 Renal malrotation HP:0004712
img Structural anomalies of the renal tract HP:0004735
img Mesangial abnormality HP:0001966
img Abnormality of the renal cortex HP:0011035
img Fatty kidney HP:0000799
img Morphological abnormalities of the glomeruli HP:0000095
img Hyperechogenic kidneys HP:0004719
img Nephrocalcinosis HP:0000121
img Unilateral renal atrophy HP:0008717
img Abnormality of the renal medulla HP:0100957
img Renal cysts HP:0000107
img Nephrolithiasis HP:0000787
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:00001186img Abnormality of the kidney HP:0000077
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the kidney HP:0000077
Genes (512)

Species:
human : 512
Page Size
Current 25
  Page 1 of 21
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanGFND1100689213Glomerulopathy with fibronectin deposits 1
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanIGAN2100653384IgA nephropathy, susceptibility to, 2
img HP RolledUp, OMIM ID: 613944
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
HumanDER22T11-22100529146
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
HumanRCHTS100462676Roifman-Chitayat syndrome
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL2P16.1-P15100240740
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanCFSS100188773craniofacioskeletal syndrome
HumanDIP100188011interstitial pneumonitis, desquamative, familial
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanMGS100126595Mungen syndrome
HumanSHFM3100049542Split-hand/foot malformation 3
img HP RolledUp, OMIM ID: 246560
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanDEL17Q21.31791085
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanCOA5493753cytochrome c oxidase assembly factor 5
HumanWG474168Wegener granulomatosis
HumanGDF6392255growth differentiation factor 6
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012210Abnormal renal morphology0self