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Details
Link-It Detail - Disease - Avitaminosis
Debug Stats
  • ### Total Build Time: 34 ms 31.474 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 202 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=2 ms Completed: 2 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.689 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.520 KB
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 7.452 KB
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 17.401 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Avitaminosis C0376286
Definition (1)
a disease due to a lack of a vitamin in the body
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Deficiency Diseases C0011156
Children (6)
img Vitamin B Deficiency C0042850
img Vitamin A Deficiency C0042842
img Vitamin D Deficiency C0042870
img Vitamin E Deficiency C0042875
img Ascorbic Acid Deficiency C0003969
img Vitamin K Deficiency C0042880
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Nutrition Disorders C00287095img Deficiency Diseases C0011156
Relationships (17)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 7
diso_​to_​diso : 7
diso_​to_​phys : 1


Relationships:
none : 13
associated_​with : 2
mapped_​to : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM39img Vitamins C0042890
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_ANAT23img In Blood C0005768
DISO_to_CHEM22img Vitamins C0042890
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_DISO11img Morbid Obesities C0028756
DISO_to_ANAT10img In Blood C0005768
DISO_to_CHEM10img Micronutrients C0282575
DISO_to_DISO10img Malnutrition C0162429
DISO_to_PHYS10img Nutritional Status C0392209
DISO_to_CHEM8img Micronutrients C0282575
DISO_to_CHEM7img Minerals C0026162
DISO_to_CHEM7img Trace Elements C0040577
DISO_to_CHEMassociated_withimg Vitamins C0042890
DISO_to_DISOmapped_toimg AVITAMINOSIS D C0042870
DISO_to_DISOmapped_toimg Avitaminosis C0376286
DISO_to_DISOassociated_withimg Malnutrition C0162429
Genes (40)

Species:
human : 40
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanAMN81693amnion associated transmembrane protein
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanBCMO153630beta-carotene 15,15'-monooxygenase 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanMTHFD1L25902methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanFGF238074fibroblast growth factor 23
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanUCP37352uncoupling protein 3 (mitochondrial, proton carrier)
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanTYMS7298thymidylate synthetase
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanTTPA7274tocopherol (alpha) transfer protein
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanTALDO16888transaldolase 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanSLC19A16573solute carrier family 19 (folate transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanSFRP46424secreted frizzled-related protein 4
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanPRL5617prolactin
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanOCRL4952oculocerebrorenal syndrome of Lowe
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanMTHFR4524methylenetetrahydrofolate reductase (NAD(P)H)
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanMTHFD14522methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanMAPT4137microtubule-associated protein tau
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
INFERRED, Score=800, UMLKSK CUI: C0376286
HumanHLA-DQB13119
INFERRED, Score=800, UMLKSK CUI: C0376286
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0376286Avitaminosis0self