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Details
Link-It Detail - Disease - Anemia, Megaloblastic
Debug Stats
  • ### Total Build Time: 144 ms 31.610 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 391 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=1 ms Completed: 1 ms rowSize= 285 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=12 ms Completed: 11 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 556 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 1.514 KB
  • CONCEPT_RELATIONSHIPS gt=82 ms Completed: 82 ms rowSize= 14.622 KB
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 12.364 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anemia, Megaloblastic C0002888
ANAEMIA MEGALOBLASTIC
Definition (1)
A disorder characterized by the presence of ANEMIA, abnormally large red blood cells (megalocytes or macrocytes), and MEGALOBLASTS.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Anemia, Macrocytic C0002886
Children (1)
img Anemia, Pernicious C0002892
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Anemia, Macrocytic C0002886
Relationships (59)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 19
diso_​to_​diso : 31
diso_​to_​gene : 2
diso_​to_​phen : 2


Relationships:
none : 10
gene_​associated_​with_​disease : 2
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 22
mapped_​to : 3
may_​be_​finding_​of_​disease : 1
may_​treat : 17
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO25img CYANOCOBALAMIN DEFICIENCY C0042847
DISO_to_DISO23img CYANOCOBALAMIN DEFICIENCY C0042847
DISO_to_PHEN21img genetic aspects C0017399
DISO_to_PHEN19img genetic aspects C0017399
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_ANAT15img In Blood C0005768
DISO_to_CHEM13img Thiamine C0039840
DISO_to_ANAT9img In Blood C0005768
DISO_to_CHEM9img Vitamin B Complex C0042849
DISO_to_DISO9img Bone Marrow Failure C0030312
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_CHEMmay_treatimg 6(S)-5-methyltetrahydrofolate C1337136
DISO_to_CHEMmay_treatimg CALCIUM FOLINATE 10MG/ML INJ C0978118
DISO_to_CHEMmay_treatimg Calcium folinate 15mg tablet C0689323
DISO_to_CHEMmay_treatimg FOLATE SODIUM 5 MG INTRAMUSCULAR INJECTION, SOLUTION C0773592
DISO_to_CHEMmay_treatimg FOLIC ACID 0.4 MG Oral (systemic) tablet C0691451
DISO_to_CHEMmay_treatimg FOLIC ACID 0.8 MG Oral (systemic) tablet C0691452
DISO_to_CHEMmay_treatimg FOLIC ACID 10 MG INTRAMUSCULAR INJECTION, SOLUTION C0977009
DISO_to_CHEMmay_treatimg Folic Acid C0016410
DISO_to_CHEMmay_treatimg Folic Acid 1 MG Oral Tablet C0977010
DISO_to_CHEMmay_treatimg Folinic acid 15mg injection C0784241
DISO_to_CHEMmay_treatimg Folinic acid 30mg/10mL injection C0792168
DISO_to_CHEMmay_treatimg LEUCOVORIN CALCIUM 10 MG ORAL TABLET C0689321
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanAMN81693amnion associated transmembrane protein
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanMMADHC27249methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanPHGDH26227phosphoglycerate dehydrogenase
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanFTCD10841formimidoyltransferase cyclodeaminase
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
img OMIM, Score=833, UMLKSK CUI: C0002888
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanWFS17466Wolfram syndrome 1 (wolframin)
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanTCN26948transcobalamin II
img GENERIF, Score=1000, Pubmed Id: 12064907, UMLKSK CUI: C0002888
HumanMTRR45525-methyltetrahydrofolate-homocysteine methyltransferase reductase
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanMTR45485-methyltetrahydrofolate-homocysteine methyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanHPRT13251hypoxanthine phosphoribosyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanGIF2694gastric intrinsic factor (vitamin B synthesis)
img OMIM, Score=1000, UMLKSK CUI: C0002888
HumanAIRE326autoimmune regulator
INFERRED, Score=800, UMLKSK CUI: C0002888
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002888Anemia, Megaloblastic0self