Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Human Phenotype - Abnormality of the menstrual cycle
Debug Stats
  • ### Total Build Time: 36 ms 30.632 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 207 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=2 ms Completed: 2 ms rowSize= 793 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.286 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 3.049 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 22.943 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the menstrual cycle HP:0000140
Definition (1)
An abnormality of the `ovulation cycle` (GO:0042698).
Parents (2)
img Abnormality of female internal genitalia HP:0000008
img Puberty and gonadal disorders HP:0008373
Children (7)
img Menorrhagia HP:0000132
img Amenorrhea HP:0000141
img Menstrual irregularities HP:0000858
img Metrorrhagia HP:0100608
img Oligomenorrhea HP:0000876
img Dysmenorrhea HP:0100607
img Hypermenorrhea HP:0100609
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
img All HP:0000001img Phenotypic abnormality HP:00001185img Puberty and gonadal disorders HP:0008373
Genes (104)

Species:
human : 104
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanDFNB81100653390deafness, autosomal recessive 81
img HP RolledUp, OMIM ID: 614129
HumanENDO1100188863Endometriosis, susceptibility to, 1
img HP RolledUp, OMIM ID: 131200
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP TAS, OMIM ID: 149000
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanNLRP7199713NLR family, pyrin domain containing 7
img HP TAS, OMIM ID: 231090
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanMCFD290411multiple coagulation factor deficiency 2
img HP RolledUp, OMIM ID: 613625
HumanKISS1R84634KISS1 receptor
img HP RolledUp, OMIM ID: 146110
HumanANTXR184168anthrax toxin receptor 1
img HP RolledUp, OMIM ID: 230740
HumanPOF1B79983premature ovarian failure, 1B
img HP RolledUp, OMIM ID: 300604
HumanPROK260675prokineticin 2
img HP RolledUp, OMIM ID: 146110
HumanWDR1155717WD repeat domain 11
img HP RolledUp, OMIM ID: 614858
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 146110
HumanAGGF155109angiogenic factor with G patch and FHA domains 1
img HP TAS, OMIM ID: 149000
HumanMAGEL254551MAGE-like 2
img HP RolledUp, OMIM ID: 176270
HumanRNF21654476ring finger protein 216
img HP RolledUp, OMIM ID: 212840
HumanWNT454361wingless-type MMTV integration site family, member 4
img HP RolledUp, OMIM ID: 277000
img HP RolledUp, OMIM ID: 158330
HumanGP651206glycoprotein VI (platelet)
img HP RolledUp, OMIM ID: 614201
HumanNIN51199ninein (GSK3B interacting protein)
img HP RolledUp, OMIM ID: 614851
HumanDHH50846desert hedgehog
img HP RolledUp, OMIM ID: 233420
HumanPSMC3IP29893PSMC3 interacting protein
img HP RolledUp, OMIM ID: 614324
HumanNSMF26012NMDA receptor synaptonuclear signaling and neuronal migration factor
img HP RolledUp, OMIM ID: 146110
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000140Abnormality of the menstrual cycle0self