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Details
Link-It Detail - Disease - Hyperparathyroidism, Primary
Debug Stats
  • ### Total Build Time: 227 ms 28.346 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 411 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 428 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=6 ms Completed: 6 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.512 KB
  • CONCEPT_RELATIONSHIPS gt=173 ms Completed: 173 ms rowSize= 13.517 KB
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 10.575 KB
  • CONCEPT_XREFS gt=17 ms Completed: 17 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hyperparathyroidism, Primary C0221002
HYPERPARATHYROIDISM PRIMARY
Definition (1)
A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hyperparathyroidism C0020502
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Parathyroid Diseases C00305174img Hyperparathyroidism C0020502
Relationships (51)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 7
diso_​to_​diso : 34
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 23
classifies : 1
clinically_​similar : 16
disease_​has_​associated_​disease : 1
is_​associated_​anatomic_​site_​of : 3
isa : 1
mapped_​to : 6
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO252img Complication Aspects C1171258
DISO_to_ANAT222img In Blood C0005768
DISO_to_DISO183img NEOPL PARATHYROID C0030521
DISO_to_CHEM120img Parathyroid Hormone C0030520
DISO_to_DISO115img Adenoma C0001430
DISO_to_DISO71img CALCIUM BLOOD INCREASED C0020437
DISO_to_PHEN64img genetic aspects C0017399
DISO_to_CHEM55img Calcium C0006675
DISO_to_ANAT50img Parathyroid Glands C0030518
DISO_to_ANAT42img In Blood C0005768
DISO_to_CHEM41img Technetium Tc 99m Sestamibi C0162680
DISO_to_DISO40img NEOPL PARATHYROID C0030521
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_CHEM30img Vitamin D C0042866
DISO_to_CHEM28img Radiopharmaceuticals C0182638
DISO_to_DISO28img Adenoma C0001430
DISO_to_DISO26img Vitamin D Deficiency C0042870
DISO_to_CHEM24img Naphthalenes C0027378
DISO_to_CHEM20img Parathyroid Hormone C0030520
DISO_to_DISO20img HYPERPARATHYROIDISM SECOND C0020503
DISO_to_DISO18img Thyroid Neoplasm C0040136
DISO_to_PHYS18img Bone Density C0005938
DISO_to_ANAT17img Parathyroid Glands C0030518
DISO_to_ANATclinically_similarimg Accessory parathyroid gland C1267791
DISO_to_ANATis_associated_anatomic_site_ofimg Head and neck structure C0460004
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanCDC7379577cell division cycle 73
img OMIM, Score=1000, UMLKSK CUI: C0221002
HumanKL9365klotho
img GENERIF, Score=1000, Pubmed Id: 18682507, UMLKSK CUI: C0221002
HumanRET5979ret proto-oncogene
img GENERIF, Score=1000, Pubmed Id: 17527003, UMLKSK CUI: C0221002
HumanPTH5741parathyroid hormone
img GAD, Score=1000, Pubmed Id: 11014383, UMLKSK CUI: C0221002
HumanMEN14221multiple endocrine neoplasia I
img OMIM, Score=1000, UMLKSK CUI: C0221002
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
img GENERIF, Score=1000, Pubmed Id: 17853647, UMLKSK CUI: C0221002
HumanCASR846calcium-sensing receptor
img GENERIF, Score=1000, Pubmed Id: 17062884, UMLKSK CUI: C0221002
img GAD, Score=1000, Pubmed Id: 11589681, UMLKSK CUI: C0221002
img OMIM, Score=882, UMLKSK CUI: C0221002
img GENERIF, Score=1000, Pubmed Id: 17853337, UMLKSK CUI: C0221002
HumanADM133adrenomedullin
img GENERIF, Score=1000, Pubmed Id: 12601625, UMLKSK CUI: C0221002
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0221002Hyperparathyroidism, Primary0self