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Details
Link-It Detail - Human Phenotype - Abnormality of the bladder
Debug Stats
  • ### Total Build Time: 35 ms 32.274 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 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=3 ms Completed: 3 ms rowSize= 795 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 4.593 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.108 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 23.234 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the bladder HP:0000014
Definition (1)
An abnormality of the `urinary bladder` (FMA:15900).
Parents (2)
img Abnormality of the lower urinary tract HP:0010936
img Abnormality of the urinary system HP:0000079
Children (14)
img Bladder exstrophy HP:0002836
img Bladder fistula HP:0004321
img Cloacal exstrophy HP:0010475
img Cystocele HP:0100645
img Urinary bladder sphincter dysfunction HP:0002839
img Lower urinary tract dilatation HP:0000021
img Hypertrophy of the urinary bladder HP:0008635
img Bladder stones HP:0010474
img Aplasia/Hypoplasia of the bladder HP:0010476
img Functional abnormality of the bladder HP:0000009
img Bladder diverticula HP:0000015
img Poor bladder function HP:0008731
img Abnormality of the urachus HP:0010478
img Dilatation of the bladder HP:0010955
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the lower urinary tract HP:0010936
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the urinary system HP:0000079
Genes (200)

Species:
human : 200
Page Size
Current 25
  Page 1 of 8
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
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
HumanSPAX3100379201Ataxia, spastic, 3, autosomal recessive
img HP RolledUp, OMIM ID: 611390
HumanSPG41100359402spastic paraplegia 41 (autosomal dominant)
img HP RolledUp, OMIM ID: 613364
HumanPVOP1100312952Pelvic organ prolapse, susceptibility to, 1
img HP RolledUp, OMIM ID: 176780
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanASDP100187749anal sphincter dysplasia
img HP RolledUp, OMIM ID: 105563
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanSPG37100049159spastic paraplegia 37 (autosomal dominant)
img HP RolledUp, OMIM ID: 611945
HumanSPG36791228spastic paraplegia 36 (autosomal dominant)
img HP RolledUp, OMIM ID: 613096
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanSPG29619379spastic paraplegia 29 (autosomal dominant)
img HP RolledUp, OMIM ID: 609727
HumanSPG27414886spastic paraplegia 27 (autosomal recessive)
img HP RolledUp, OMIM ID: 609041
HumanSCA25338435spinocerebellar ataxia 25
img HP RolledUp, OMIM ID: 608703
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP RolledUp, OMIM ID: 181270
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanSLSN3260432Senior-Loken syndrome 3
img HP RolledUp, OMIM ID: 606995
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000014Abnormality of the bladder0self