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Details
Link-It Detail - Disease - Puberty, Precocious
Debug Stats
  • ### Total Build Time: 66 ms 36.502 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 335 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 553 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.507 KB
  • CONCEPT_RELATIONSHIPS gt=48 ms Completed: 48 ms rowSize= 13.570 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 18.811 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Puberty, Precocious C0034013
Precocious Puberty
Definition (1)
A disorder characterized by unusually early development of secondary sexual features; the onset of sexual maturation begins usually before age 8 for girls and before age 9 for boys.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Gonadal Disorders C0018050
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Gonadal Disorders C00180503img Gonadal Disorders C0018050
Relationships (87)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 49
diso_​to_​diso : 29
diso_​to_​phen : 2
diso_​to_​phys : 4


Relationships:
none : 26
associated_​with : 1
disease_​has_​finding : 1
isa : 11
location_​of : 1
mapped_​to : 6
may_​treat : 41
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT76img In Blood C0005768
DISO_to_CHEM55img Gonadorelin C0023610
DISO_to_CHEM54img Gonadorelin C0023610
DISO_to_PHEN52img genetic aspects C0017399
DISO_to_ANAT51img In Blood C0005768
DISO_to_DISO51img Complication Aspects C1171258
DISO_to_PHEN49img genetic aspects C0017399
DISO_to_DISO32img Complication Aspects C1171258
DISO_to_DISO26img chemically induced C0007994
DISO_to_PHYS25img Puberty C0034011
DISO_to_PHYS23img Puberty C0034011
DISO_to_PHYS21img Body Height C0005890
DISO_to_CHEM18img Leuprolide C0085272
DISO_to_DISO18img Puberty, Delayed C0034012
DISO_to_CHEM17img Leuprolide C0085272
DISO_to_CHEM17img Triptorelin Pamoate C1137102
DISO_to_DISO17img Fibrous Dysplasia, Polyostotic C0016065
DISO_to_CHEM16img Luteinizing Hormone C0023607
DISO_to_CHEM15img Triptorelin Pamoate C1137102
DISO_to_DISO15img Hypothalamic Diseases C0020655
DISO_to_CHEM14img Adrenarche C0686792
DISO_to_DISO14img 755-756 HAMARTOMAS C0018552
DISO_to_DISO14img Developmental Disabilities C0008073
DISO_to_DISO14img Fibrous Dysplasia, Polyostotic C0016065
DISO_to_DISO14img HYPOTHYROIDISM C0020676
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanRAB2351715RAB23, member RAS oncogene family
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanTSC27249tuberous sclerosis 2
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanTSC17248tuberous sclerosis 1
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanSTK116794serine/threonine kinase 11
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanSERPINE15054serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
img GENERIF, Score=658, Pubmed Id: 11809921, UMLKSK CUI: C0034013
HumanLHCGR3973luteinizing hormone/choriogonadotropin receptor
img GENERIF, Score=913, Pubmed Id: 18772599, UMLKSK CUI: C0034013
img OMIM, Score=833, UMLKSK CUI: C0034013
HumanKISS13814KiSS-1 metastasis-suppressor
img GENERIF, Score=1000, Pubmed Id: 17609410, UMLKSK CUI: C0034013
HumanIRS13667insulin receptor substrate 1
img GAD, Score=1000, Pubmed Id: 12477526, UMLKSK CUI: C0034013
HumanINSR3643insulin receptor
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
img GENERIF, Score=865, Pubmed Id: 18675202, UMLKSK CUI: C0034013
HumanIFNG3458interferon, gamma
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanGNAS2778GNAS complex locus
img GENERIF, Score=861, Pubmed Id: 17982386, UMLKSK CUI: C0034013
img GENERIF, Score=861, Pubmed Id: 15126527, UMLKSK CUI: C0034013
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanESR12099estrogen receptor 1
img GENERIF, Score=1000, Pubmed Id: 16252695, UMLKSK CUI: C0034013
HumanCYP11B11584cytochrome P450, family 11, subfamily B, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0034013
HumanCOMT1312catechol-O-methyltransferase
img GENERIF, Score=682, Pubmed Id: 15985686, UMLKSK CUI: C0034013
HumanCOL1A11277collagen, type I, alpha 1
img GENERIF, Score=1000, Pubmed Id: 16580273, UMLKSK CUI: C0034013
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0034013Puberty, Precocious0self