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Details
Link-It Detail - Human Phenotype - Abnormality of the female genitalia
Debug Stats
  • ### Total Build Time: 47 ms 24.296 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 209 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= 791 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 806 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.104 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 19.049 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.029 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the female genitalia HP:0010460
Definition (1)
Abnormality of the `female genital system` (FMA:45663).
Parents (2)
img Abnormality of the genital system HP:0000078
img Abnormal genital system morphology HP:0012243
Children (2)
img Abnormality of female internal genitalia HP:0000008
img Abnormality of female external genitalia HP:0000055
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the genital system HP:0000078
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal genital system morphology HP:0012243
Genes (299)

Species:
human : 299
Page Size
Current 25
  Page 1 of 12
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanDFNB81100653390deafness, autosomal recessive 81
img HP RolledUp, OMIM ID: 614129
HumanDEL11P13100528024Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
HumanCRCS10100271691Colorectal cancer, susceptibility to, 10
img HP RolledUp, OMIM ID: 612591
HumanIBD25100270799Inflammatory bowel disease-25
img HP RolledUp, OMIM ID: 612567
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanENDO1100188863Endometriosis, susceptibility to, 1
img HP RolledUp, OMIM ID: 131200
HumanSNORD116-1100033413
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
HumanGDF6392255growth differentiation factor 6
img HP RolledUp, OMIM ID: 122600
HumanKIF7374654kinesin family member 7
HumanFIGLA344018folliculogenesis specific basic helix-loop-helix
img HP RolledUp, OMIM ID: 612310
HumanFREM2341640FRAS1 related extracellular matrix protein 2
HumanSNORD115-1338433
HumanHYLS1219844hydrolethalus syndrome 1
HumanFLCN201163folliculin
HumanNLRP7199713NLR family, pyrin domain containing 7
img HP RolledUp, OMIM ID: 231090
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanBBS12166379Bardet-Biedl syndrome 12
HumanFREM1158326FRAS1 related extracellular matrix 1
img HP RolledUp, OMIM ID: 608980
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010460Abnormality of the female genitalia0self