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Details
Link-It Detail - Disease - Calcium Metabolism Disorders
Debug Stats
  • ### Total Build Time: 91 ms 37.765 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 258 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=14 ms Completed: 14 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= 554 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.080 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.518 KB
  • CONCEPT_RELATIONSHIPS gt=49 ms Completed: 49 ms rowSize= 13.207 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 17.448 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Calcium Metabolism Disorders C0006705
Definition (1)
Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Metabolic Diseases C0025517
Children (7)
img Decalcification, Pathologic C0011085
img Osteomalacia C0029442
img Hypocalcemia C0020598
img Hypercalcemia C0020437
img Calcinosis C0006663
img Pseudohypoparathyroidism C0033806
img Rickets C0035579
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255173img Metabolic Diseases C0025517
Relationships (34)

Relation Types:
diso_​to_​chem : 3
diso_​to_​diso : 29
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 6
associated_​with : 3
classifies : 2
entry_​version_​of : 1
isa : 2
mapped_​to : 19
used_​for : 1
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM29img Calcium C0006675
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_DISO14img Complication Aspects C1171258
DISO_to_CHEM13img Calcium C0006675
DISO_to_DISO11img Dis phosphorus metabol C0031707
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_CHEMassociated_withimg Calcium C0006675
DISO_to_DISOclassifiesimg 6-30 DISORDERS OF MINERAL METABOLISM: GENERAL TERMS C0154260
DISO_to_DISOmapped_toimg CALCIFICATION METASTATIC C0221255
DISO_to_DISOmapped_toimg CALCINOSIS RENAL C0027709
DISO_to_DISOmapped_toimg CALCIUM BLOOD INCREASED C0020437
DISO_to_DISOused_forimg CALCIUM DISORDER C0302590
DISO_to_DISOentry_version_ofimg CALCIUM METAB DIS C0006705
DISO_to_DISOmapped_toimg Calcinosis C0006663
DISO_to_DISOmapped_toimg Calcium pyrophosphate deposition disease C0553730
DISO_to_DISOassociated_withimg Disease C0012634
DISO_to_DISOmapped_toimg HYPERCALCEMIA, IDIOPATHIC, OF INFANCY C0268080
DISO_to_DISOisaimg HYPERCALCINURIA C0020438
DISO_to_DISOmapped_toimg Hydroxyapatite arthropathy C0268081
DISO_to_DISOmapped_toimg Hypercalciuria C0020438
DISO_to_DISOmapped_toimg Hypocalcemia C0020598
DISO_to_DISOmapped_toimg Hypocalciuria C0020599
DISO_to_DISOmapped_toimg Idiopathic articular chondrocalcinosis C0409895
DISO_to_DISOmapped_toimg Idiopathic hypercalciuria with bilateral macular colobomata C2931121
DISO_to_DISOisaimg Nephrocalcinosis C0027709
Genes (65)

Species:
human : 65
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanCLDN19149461claudin 19
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanCDC7379577cell division cycle 73
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanSAMD954809sterile alpha motif domain containing 9
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanOSTM128962osteopetrosis associated transmembrane protein 1
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanVPS33B26276vacuolar protein sorting 33 homolog B (yeast)
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanIBGC123706idiopathic basal ganglia calcification 1
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanKIF1B23095kinesin family member 1B
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanCLDN1610686claudin 16
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanKL9365klotho
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanGCM29247glial cells missing homolog 2 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanFGF238074fibroblast growth factor 23
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanVHL7428von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTRH7200thyrotropin-releasing hormone
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTNNI17135troponin I type 1 (skeletal, slow)
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTCF36929transcription factor 3
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTBCE6905tubulin folding cofactor E
INFERRED, Score=800, UMLKSK CUI: C0006705
HumanTBX16899T-box 1
INFERRED, Score=800, UMLKSK CUI: C0006705
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0006705Calcium Metabolism Disorders0self