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Details
Link-It Detail - Disease - Amenorrhea
Debug Stats
  • ### Total Build Time: 87 ms 27.192 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 318 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 178 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= 240 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.535 KB
  • CONCEPT_RELATIONSHIPS gt=72 ms Completed: 72 ms rowSize= 13.750 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 9.461 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Amenorrhea C0002453
Definition (1)
Absence of menstruation.
Semantic Types (2)
Disease or Syndrome (T047)
Sign or Symptom (T184)
Parents (1)
img Menstruation Disturbances C0025345
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Menstruation Disturbances C0025345
Relationships (114)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 49
diso_​to_​diso : 49
diso_​to_​phen : 2
diso_​to_​phys : 7


Relationships:
none : 39
classifies : 1
disease_​may_​have_​finding : 10
isa : 1
mapped_​to : 19
may_​treat : 43
use : 1
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT60img In Blood C0005768
DISO_to_DISO57img chemically induced C0007994
DISO_to_PHEN54img genetic aspects C0017399
DISO_to_DISO37img chemically induced C0007994
DISO_to_DISO35img Osteoporosis C0029456
DISO_to_DISO34img Breast Neoplasms C1458155
DISO_to_ANAT32img In Blood C0005768
DISO_to_DISO31img Eating Disorders C0013473
DISO_to_DISO30img Complication Aspects C1171258
DISO_to_DISO30img Hypothalamic Diseases C0020655
DISO_to_DISO22img Polycystic Ovary Syndrome C0032460
DISO_to_DISO21img Complication Aspects C1171258
DISO_to_PHYS19img Menstruation C0025344
DISO_to_DISO17img Anorexia Nervosa C0003125
DISO_to_DISO17img Oligomenorrhea C0028949
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_DISO16img Breast Neoplasms C1458155
DISO_to_DISO16img Hypothalamic Diseases C0020655
DISO_to_PHYS15img Bone Density C0005938
DISO_to_ANAT13img Uterus C0042149
DISO_to_DISO13img Anorexia Nervosa C0003125
DISO_to_DISO13img Eating Disorders C0013473
DISO_to_PHYS13img Lactation C0022925
DISO_to_CHEM12img Antineoplastic Agents C0003392
DISO_to_DISO12img Oligomenorrhea C0028949
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanWNT454361wingless-type MMTV integration site family, member 4
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanGHRL51738ghrelin/obestatin prepropeptide
img GENERIF, Score=1000, Pubmed Id: 18001718, UMLKSK CUI: C0002453
HumanFST10468follistatin
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanWNT7A7476wingless-type MMTV integration site family, member 7A
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanNPY4852neuropeptide Y
img GENERIF, Score=861, Pubmed Id: 16136022, UMLKSK CUI: C0002453
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanLEP3952leptin
img GENERIF, Score=861, Pubmed Id: 16136022, UMLKSK CUI: C0002453
HumanFOXL2668forkhead box L2
img OMIM, Score=1000, UMLKSK CUI: C0002453
HumanBMP2650bone morphogenetic protein 2
img OMIM, Score=1000, UMLKSK CUI: C0002453
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002453Amenorrhea0self