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Details
Link-It Detail - Human Phenotype - Abnormality of the ovary
Debug Stats
  • ### Total Build Time: 47 ms 30.040 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 195 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= 461 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 3.282 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=15 ms Completed: 15 ms rowSize= 2.117 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 22.643 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the ovary HP:0000137
Definition (1)
An abnormality of the `ovary` (FMA:7209).
Parents (1)
img Abnormality of female internal genitalia HP:0000008
Children (10)
img Female hypogonadism HP:0000134
img Ovarian cysts HP:0000138
img Primary ovarian failure HP:0001587
img Ovarian neoplasm HP:0100615
img Premature ovarian failure HP:0008209
img Enlarged ovaries HP:0100879
img Ovarian cystic abnormality HP:0000146
img Ovarian gonadoblastoma HP:0000149
img Aplasia/Hypoplasia of the ovary HP:0010462
img Ovarian fibroma HP:0010618
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of female internal genitalia HP:0000008
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of female internal genitalia HP:0000008
Genes (96)

Species:
human : 96
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanDEL11P13100528024Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
img HP RolledUp, OMIM ID: 194072
HumanFIGLA344018folliculogenesis specific basic helix-loop-helix
img HP RolledUp, OMIM ID: 612310
HumanBBS12166379Bardet-Biedl syndrome 12
img HP IEA, OMIM ID: 209900
HumanNOBOX135935NOBOX oogenesis homeobox
img HP RolledUp, OMIM ID: 611548
HumanBBS5129880Bardet-Biedl syndrome 5
img HP IEA, OMIM ID: 209900
HumanTTC8123016tetratricopeptide repeat domain 8
img HP IEA, OMIM ID: 209900
HumanANTXR2118429anthrax toxin receptor 2
img HP RolledUp, OMIM ID: 236490
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanTMEM6791147transmembrane protein 67
img HP IEA, OMIM ID: 209900
HumanLMNB284823lamin B2
img HP RolledUp, OMIM ID: 608709
HumanARL684100ADP-ribosylation factor-like 6
img HP IEA, OMIM ID: 209900
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP RolledUp, OMIM ID: 224750
HumanCEP29080184centrosomal protein 290kDa
img HP IEA, OMIM ID: 209900
HumanDCAF1780067DDB1 and CUL4 associated factor 17
img HP RolledUp, OMIM ID: 241080
HumanPOF1B79983premature ovarian failure, 1B
img HP RolledUp, OMIM ID: 300604
HumanBBS1079738Bardet-Biedl syndrome 10
img HP IEA, OMIM ID: 209900
HumanCCDC28B79140coiled-coil domain containing 28B
img HP IEA, OMIM ID: 209900
HumanC10orf256652chromosome 10 open reading frame 2
img HP RolledUp, OMIM ID: 609286
HumanBBS755212Bardet-Biedl syndrome 7
img HP IEA, OMIM ID: 209900
HumanMKS154903Meckel syndrome, type 1
img HP IEA, OMIM ID: 209900
HumanRAB4B53916RAB4B, member RAS oncogene family
img HP RolledUp, OMIM ID: 612945
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanWDPCP51057WD repeat containing planar cell polarity effector
img HP IEA, OMIM ID: 209900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000137Abnormality of the ovary0self