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Details
Link-It Detail - Disease - Hyperparathyroidism, Secondary
Debug Stats
  • ### Total Build Time: 128 ms 23.480 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 414 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 408 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=10 ms Completed: 10 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 558 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=22 ms Completed: 22 ms rowSize= 1.512 KB
  • CONCEPT_RELATIONSHIPS gt=68 ms Completed: 68 ms rowSize= 12.113 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 6.591 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hyperparathyroidism, Secondary C0020503
HYPERPARATHYROIDISM SECOND
Definition (1)
Abnormally elevated PARATHYROID HORMONE secretion as a response to HYPOCALCEMIA. It is caused by chronic KIDNEY FAILURE or other abnormalities in the controls of bone and mineral metabolism, leading to various BONE DISEASES, such as RENAL OSTEODYSTROPHY.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hyperparathyroidism C0020502
Children (1)
img Renal Osteodystrophy C0035086
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Parathyroid Diseases C00305174img Hyperparathyroidism C0020502
Relationships (31)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 12
diso_​to_​diso : 15


Relationships:
none : 22
clinically_​similar : 8
isa : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO191img Kidney Failure, Chronic C0022661
DISO_to_ANAT170img In Blood C0005768
DISO_to_DISO154img Kidney Failure, Chronic C0022661
DISO_to_CHEM147img Naphthalenes C0027378
DISO_to_ANAT135img In Blood C0005768
DISO_to_DISO101img Complication Aspects C1171258
DISO_to_DISO93img Complication Aspects C1171258
DISO_to_CHEM91img Parathyroid Hormone C0030520
DISO_to_CHEM89img Parathyroid Hormone C0030520
DISO_to_ANAT82img Parathyroid Glands C0030518
DISO_to_ANAT73img Parathyroid Glands C0030518
DISO_to_CHEM70img Calcitriol C0006674
DISO_to_CHEM65img Vitamin D C0042866
DISO_to_DISO60img Kidney Diseases C0022658
DISO_to_DISO57img Vitamin D Deficiency C0042870
DISO_to_CHEM50img Naphthalenes C0027378
DISO_to_CHEM49img Calcium C0006675
DISO_to_CHEM43img Calciferols C0014696
DISO_to_CHEM43img Calcitriol C0006674
DISO_to_CHEM39img Vitamin D C0042866
DISO_to_CHEM33img Bone Density Conservation Agents C1563726
DISO_to_CHEM33img Calcium C0006675
DISO_to_DISOclinically_similarimg HPTH - Hyperparathyroidism C0020502
DISO_to_DISOclinically_similarimg HYPERPARATHYROIDISM SECOND C0020503
DISO_to_DISOisaimg Hyperparathyroidism due to 1,25(0H)2 D3 C0271848
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img GENERIF, Score=1000, Pubmed Id: 15848611, UMLKSK CUI: C0020503
img GENERIF, Score=694, Pubmed Id: 12649542, UMLKSK CUI: C0020503
img GENERIF, Score=1000, Pubmed Id: 12369780, UMLKSK CUI: C0020503
img OMIM, Score=1000, UMLKSK CUI: C0020503
img OMIM, Score=1000, UMLKSK CUI: C0020503
HumanOCRL4952oculocerebrorenal syndrome of Lowe
INFERRED, Score=800, UMLKSK CUI: C0020503
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0020503
img OMIM, Score=1000, UMLKSK CUI: C0020503
HumanACP554acid phosphatase 5, tartrate resistant
INFERRED, Score=800, UMLKSK CUI: C0020503
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020503Hyperparathyroidism, Secondary0self