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Details
Link-It Detail - Disease - Hyperthyroxinemia
Debug Stats
  • ### Total Build Time: 79 ms 10.748 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 203 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=17 ms Completed: 17 ms rowSize= 1.009 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=29 ms Completed: 29 ms rowSize= 4.144 KB
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 1.667 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperthyroxinemia C0020551
Definition (1)
Abnormally elevated THYROXINE level in the BLOOD.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Thyroid Diseases C0040128
Children (2)
img Hyperthyroxinemia, Familial Dysalbuminemic C0342185
img Thyroid Hormone Resistance Syndrome C0242604
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Thyroid Diseases C00401283img Thyroid Diseases C0040128
Relationships (7)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 2
diso_​to_​diso : 3
diso_​to_​phen : 1


Relationships:
none : 4
mapped_​to : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT4img In Blood C0005768
DISO_to_CHEM4img Serum Albumin C0036773
DISO_to_CHEM4img Thyroxine C0040165
DISO_to_PHEN4img genetic aspects C0017399
DISO_to_DISOmapped_toimg Dystransthyretinemic Euthyroidal Hyperthyroxinemia C2750824
DISO_to_DISOpermuted_term_ofimg Hyperthyroxinemia C0020551
DISO_to_DISOmapped_toimg THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT C1861101
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanTSHR7253thyroid stimulating hormone receptor
INFERRED, Score=800, UMLKSK CUI: C0020551
HumanTHRB7068thyroid hormone receptor, beta
INFERRED, Score=800, UMLKSK CUI: C0020551
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020551Hyperthyroxinemia0self