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Details
Link-It Detail - Human Phenotype - Abnormality of the genitourinary system
Debug Stats
  • ### Total Build Time: 91 ms 28.482 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 214 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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= 443 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.751 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.158 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=89 ms Completed: 89 ms rowSize= 23.530 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.033 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the genitourinary system HP:0000119
Definition (1)
The presence of any abnormality of the `genitourinary system` (FMA:280610).
Parents (1)
img Phenotypic abnormality HP:0000118
Children (5)
img Neoplasm of the genitourinary tract HP:0007379
img Genitourinary tract malformation HP:0008713
img Abnormality of the genital system HP:0000078
img Abnormality of the urinary system HP:0000079
img Genitourinary dysplasia HP:0008688
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (1345)

Species:
human : 1345
Page Size
Current 25
  Page 1 of 54
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOPHLC101290499Omphalocele due to duplication of 1p31.3
img HP RolledUp, OMIM ID: 164750
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanSPGFX2100820759Spermatogenic failure, X-linked, 2
img HP RolledUp, OMIM ID: 309120
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanHNFJ3100689490Hyperuricemic nephropathy, familial juvenile, 3
img HP RolledUp, OMIM ID: 614227
HumanGFND1100689213Glomerulopathy with fibronectin deposits 1
img HP RolledUp, OMIM ID: 137950
HumanHYSP3100689211Hypospadias 3, autosomal
img HP RolledUp, OMIM ID: 146450
HumanHPPD100682260Hypertelorism, preauricular sinus, punctal pits, and deafness
img HP RolledUp, OMIM ID: 614187
HumanDFNB81100653390deafness, autosomal recessive 81
img HP RolledUp, OMIM ID: 614129
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanIGAN2100653384IgA nephropathy, susceptibility to, 2
img HP RolledUp, OMIM ID: 613944
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanSRXX210065337846XX sex reversal 2
img HP RolledUp, OMIM ID: 278850
HumanSRXX310065337246XX sex reversal 3
img HP RolledUp, OMIM ID: 300833
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
img HP RolledUp, OMIM ID: 612530
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000119Abnormality of the genitourinary system0self