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Details
Link-It Detail - Disease - Choline Deficiency
Debug Stats
  • ### Total Build Time: 120 ms 14.385 KB
  • CONCEPT_NAME gt=16 ms Completed: 16 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 718 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=4 ms Completed: 4 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=26 ms Completed: 26 ms rowSize= 1.521 KB
  • CONCEPT_RELATIONSHIPS gt=54 ms Completed: 54 ms rowSize= 8.143 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 1.780 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Choline Deficiency C0008412
Definition (1)
A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984)
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 (19)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 8
diso_​to_​diso : 7
diso_​to_​phen : 1


Relationships:
none : 14
may_​treat : 4
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO45img Fatty Liver C0015695
DISO_to_CHEM42img Methionine C0025646
DISO_to_DISO37img Complication Aspects C1171258
DISO_to_DISO24img Complication Aspects C1171258
DISO_to_ANAT17img Liver C0023884
DISO_to_CHEM17img Choline C0008405
DISO_to_DISO14img Fatty Liver C0015695
DISO_to_ANAT13img Liver C0023884
DISO_to_PHEN13img genetic aspects C0017399
DISO_to_CHEM10img Choline C0008405
DISO_to_DISO10img Folic Acid Deficiency C0016412
DISO_to_ANAT9img In Blood C0005768
DISO_to_CHEM9img Methionine C0025646
DISO_to_DISO7img Liver Cirrhosis C0023890
DISO_to_CHEMmay_treatimg CHOLINE 300MG ORAL TABLET C0975626
DISO_to_CHEMmay_treatimg CHOLINE 500 MG Oral (systemic) tablet C0691331
DISO_to_CHEMmay_treatimg COLOINE C2366001
DISO_to_CHEMmay_treatimg Choline C0008405
DISO_to_DISOpermuted_term_ofimg CHOLINE DEFIC C0008412
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanMTHFD14522methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
img GENERIF, Score=1000, Pubmed Id: 16236726, UMLKSK CUI: C0008412
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0008412Choline Deficiency0self