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Details
Link-It Detail - Disease - Nutrition Disorders
Debug Stats
  • ### Total Build Time: 328 ms 38.122 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 236 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=0 Completed: 0 ms rowSize= 570 bytes
  • CONCEPT_CHILDREN gt=26 ms Completed: 26 ms rowSize= 2.676 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.137 KB
  • CONCEPT_RELATIONSHIPS gt=209 ms Completed: 209 ms rowSize= 13.436 KB
  • CONCEPT_GENES gt=78 ms Completed: 78 ms rowSize= 18.395 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Nutrition Disorders C0028709
Definition (1)
disorders caused by nutritional imbalance, either overnutrition or undernutrition.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Nutritional and Metabolic Diseases C0028715
Children (6)
img Child Nutrition Disorders C0008087
img Infant Nutrition Disorders C0021280
img Hypervitaminosis A C0020579
img Malnutrition C0162429
img Overnutrition C1257763
img Wasting Syndrome C0043046
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C00287152img Nutritional and Metabolic Diseases C0028715
Relationships (88)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 23
diso_​to_​diso : 43
diso_​to_​phen : 1
diso_​to_​phys : 18


Relationships:
none : 56
associated_​with : 1
entry_​version_​of : 1
isa : 14
may_​prevent : 8
may_​treat : 8
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO159img Complication Aspects C1171258
DISO_to_PHYS140img Nutritional Status C0392209
DISO_to_PHYS64img Nutritional Status C0392209
DISO_to_PHYS58img Nutritional Physiological Phenomena C1720791
DISO_to_ANAT51img In Blood C0005768
DISO_to_DISO49img Complication Aspects C1171258
DISO_to_CHEM39img Micronutrients C0282575
DISO_to_PHYS39img Aging C0001811
DISO_to_DISO29img Kidney Failure, Chronic C0022661
DISO_to_DISO24img Obesity C0028754
DISO_to_DISO23img Pregnancy Complications C0032962
DISO_to_DISO18img Inflammation C0021368
DISO_to_DISO17img Growth Disorders C0018273
DISO_to_PHYS17img Child Nutritional Physiological Phenomena C1720755
DISO_to_DISO16img HIV Infections C0019693
DISO_to_PHYS16img Concept, Nutrition Physiological C1720791
DISO_to_DISO15img COMPL POSTOP C0032787
DISO_to_PHEN15img genetic aspects C0017399
DISO_to_DISO14img DELAYED EFF PRENATAL EXPOSURE C0033054
DISO_to_DISO14img Neoplasms C0027651
DISO_to_DISO14img Weight Loss C0043096
DISO_to_PHYS14img Body Composition C0005885
DISO_to_PHYS14img Eating C0013470
DISO_to_PHYS14img Nutrient requirement C0028719
DISO_to_CHEM13img Micronutrients C0282575
Genes (413)

Species:
human : 413
Page Size
Current 25
  Page 1 of 17
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanZGLP1100125288zinc finger, GATA-like protein 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanLOC648998648998
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanOB4404683Obesity, susceptibility to, on chromosome 4
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanOB10Q353126Obesity, susceptibility to, on chromosome 10q
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanSNORD115-1338433
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanTUSC5286753tumor suppressor candidate 5
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanANKK1255239ankyrin repeat and kinase domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanSLC41A1254428solute carrier family 41 (magnesium transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanCAQ14171512Circulating adiponectin QTL on chromosome 14
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanTMEM74157753transmembrane protein 74
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanCCDC80151887coiled-coil domain containing 80
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanPTPRVP148713protein tyrosine phosphatase, receptor type, V, pseudogene
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanSERPINA12145264serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanGPR119139760G protein-coupled receptor 119
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanLYPLAL1127018lysophospholipase-like 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanNIPA1123606non imprinted in Prader-Willi/Angelman syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanSP7121340Sp7 transcription factor
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0028709
HumanAPOA5116519apolipoprotein A-V
INFERRED, Score=800, UMLKSK CUI: C0028709
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0028709Nutrition Disorders0self