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Details
Link-It Detail - Human Phenotype - Abnormality of prenatal development or birth
Debug Stats
  • ### Total Build Time: 49 ms 31.275 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 219 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 328 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=1 ms Completed: 1 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=3 ms Completed: 3 ms rowSize= 3.949 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=42 ms Completed: 42 ms rowSize= 24.019 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of prenatal development or birth HP:0001197
Definition (1)
Because of the close link between prenatal developmental abnormalities and abnormalities of the birth process, a single term is chosen to subsume both classes of abnormality.
Parents (1)
img Phenotypic abnormality HP:0000118
Children (12)
img Prenatal movement abnormality HP:0001557
img Abnormal delivery HP:0001787
img Premature birth HP:0001622
img Stillbirth HP:0001624
img Fetal ascites HP:0001791
img Hydrops fetalis HP:0001789
img Fetal ultrasound soft marker HP:0011425
img Increased nuchal translucency HP:0010880
img Abnormality of the amniotic fluid HP:0001560
img Spontaneous abortion HP:0005268
img Abnormalities of placenta and umbilical cord HP:0001194
img Prenatal maternal abnormality HP:0002686
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (304)

Species:
human : 304
Page Size
Current 25
  Page 1 of 13
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanCFTDX100188765Myopathy, congenital, with fiber-type disproportion, X-linked
img HP RolledUp, OMIM ID: 300580
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanISPD729920isoprenoid synthase domain containing
img HP RolledUp, OMIM ID: 614643
HumanLOC619409619409muscular dystrophy, congenital, merosin-positive
img HP RolledUp, OMIM ID: 609456
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 604131
HumanAGRN375790agrin
img HP RolledUp, OMIM ID: 254300
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanDOK7285489docking protein 7
img HP RolledUp, OMIM ID: 254300
img HP RolledUp, OMIM ID: 208150
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 604317
img HP RolledUp, OMIM ID: 600176
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
img HP RolledUp, OMIM ID: 225753
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001197Abnormality of prenatal development or birth0self