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Details
Link-It Detail - Disease - Deficiency Diseases
Debug Stats
  • ### Total Build Time: 226 ms 37.784 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 440 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= 548 bytes
  • CONCEPT_CHILDREN gt=13 ms Completed: 13 ms rowSize= 2.236 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.513 KB
  • CONCEPT_RELATIONSHIPS gt=165 ms Completed: 165 ms rowSize= 12.906 KB
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 18.472 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Deficiency Diseases C0011156
Definition (1)
A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Malnutrition C0162429
Children (5)
img Magnesium Deficiency C0024473
img Protein Deficiency C0033626
img Potassium Deficiency C0032827
img Avitaminosis C0376286
img Swayback C0038981
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Nutrition Disorders C00287094img Malnutrition C0162429
Relationships (75)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 64
diso_​to_​diso : 5
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 26
may_​diagnose : 1
may_​prevent : 20
may_​treat : 27
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO58img Complication Aspects C1171258
DISO_to_ANAT40img In Blood C0005768
DISO_to_CHEM37img Zinc C0043481
DISO_to_DISO34img Complication Aspects C1171258
DISO_to_CHEM33img Zinc C0043481
DISO_to_CHEM32img Iodine C0021968
DISO_to_CHEM30img Iodine C0021968
DISO_to_CHEM28img Micronutrients C0282575
DISO_to_PHYS23img Nutritional Status C0392209
DISO_to_ANAT22img In Blood C0005768
DISO_to_CHEM19img Micronutrients C0282575
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_CHEM15img Copper C0009968
DISO_to_CHEM12img Copper C0009968
DISO_to_CHEM12img Iron C0302583
DISO_to_CHEM12img Selenium C0036581
DISO_to_DISO12img Pregnancy Complications C0032962
DISO_to_CHEM11img Iron C0302583
DISO_to_DISO11img Morbid Obesities C0028756
DISO_to_CHEM10img Trace Elements C0040577
DISO_to_CHEM9img Minerals C0026162
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_PHYS8img Nutritional Status C0392209
DISO_to_CHEM7img Fatty Acids, Omega-3 C0015689
DISO_to_CHEM7img Selenium C0036581
Genes (52)

Species:
human : 52
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC41A1254428solute carrier family 41 (magnesium transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanAMN81693amnion associated transmembrane protein
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanBCMO153630beta-carotene 15,15'-monooxygenase 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanMTHFD1L25902methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanPROZ8858protein Z, vitamin K-dependent plasma glycoprotein
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanFGF238074fibroblast growth factor 23
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanUCP37352uncoupling protein 3 (mitochondrial, proton carrier)
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanTYMS7298thymidylate synthetase
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanTTPA7274tocopherol (alpha) transfer protein
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanTALDO16888transaldolase 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSLC19A16573solute carrier family 19 (folate transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSHBG6462sex hormone-binding globulin
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSFRP46424secreted frizzled-related protein 4
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanSCT6343secretin
img GENERIF, Score=1000, Pubmed Id: 18280672, UMLKSK CUI: C0011156
HumanPRL5617prolactin
INFERRED, Score=800, UMLKSK CUI: C0011156
HumanPOU1F15449POU class 1 homeobox 1
img GENERIF, Score=901, Pubmed Id: 15928241, UMLKSK CUI: C0011156
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED, Score=800, UMLKSK CUI: C0011156
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011156Deficiency Diseases0self