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Details
Link-It Detail - Disease - Riboflavin Deficiency
Debug Stats
  • ### Total Build Time: 34 ms 17.017 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 385 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 415 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=3 ms Completed: 3 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 1.521 KB
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 8.028 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 4.770 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Riboflavin Deficiency C0035528
ARIBOFLAVINOSIS
Definition (1)
A dietary deficiency of riboflavin causing a syndrome chiefly marked by cheilitis, angular stomatitis, glossitis associated with a purplish red or magenta-colored tongue that may show fissures, corneal vascularization, dyssebacia, and anemia. (Dorland, 27th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Vitamin B Deficiency C0042850
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Nutrition Disorders C00287097img Vitamin B Deficiency C0042850
Relationships (16)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 10
diso_​to_​diso : 5


Relationships:
none : 3
associated_​with : 1
classifies : 2
isa : 1
mapped_​to : 1
may_​prevent : 4
may_​treat : 3
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM9img Riboflavin C0035527
DISO_to_ANAT8img In Blood C0005768
DISO_to_CHEM8img Riboflavin C0035527
DISO_to_CHEMmay_preventimg Flavin Mononucleotide C0016388
DISO_to_CHEMmay_preventimg Flavin Mononucleotide 50 MG/ML Injectable Solution C0980000
DISO_to_CHEMmay_treatimg Flavin Mononucleotide Sodium Salt C0037548
DISO_to_CHEMmay_preventimg RIBOFLAVIN 100MG ORAL TABLET C0704131
DISO_to_CHEMmay_preventimg RIBOFLAVIN 10MG ORAL TABLET C0704128
DISO_to_CHEMmay_treatimg RIBOFLAVIN 25MG ORAL TABLET C0704129
DISO_to_CHEMmay_treatimg RIBOFLAVIN 50MG ORAL TABLET C0704130
DISO_to_CHEMassociated_withimg Riboflavin C0035527
DISO_to_DISOpermuted_term_ofimg ARIBOFLAVINOSIS C0035528
DISO_to_DISOisaimg Gopalan's syndrome C0006429
DISO_to_DISOmapped_toimg Inadequate dietary intake of riboflavin C2316094
DISO_to_DISOclassifiesimg Malnutrition C0162429
DISO_to_DISOclassifiesimg Other malnutrition C0810253
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanUCP37352uncoupling protein 3 (mitochondrial, proton carrier)
img GENERIF, Score=893, Pubmed Id: 14671191, UMLKSK CUI: C0035528
HumanETFDH2110electron-transferring-flavoprotein dehydrogenase
img GENERIF, Score=893, Pubmed Id: 17584774, UMLKSK CUI: C0035528
HumanETFA2108electron-transfer-flavoprotein, alpha polypeptide
img GENERIF, Score=901, Pubmed Id: 17689999, UMLKSK CUI: C0035528
HumanAPOB338apolipoprotein B
img GENERIF, Score=1000, Pubmed Id: 15867268, UMLKSK CUI: C0035528
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035528Riboflavin Deficiency0self