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Details
Link-It Detail - Disease - Anemia, Pernicious
Debug Stats
  • ### Total Build Time: 55 ms 23.104 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 347 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= 998 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.806 KB
  • CONCEPT_RELATIONSHIPS gt=38 ms Completed: 38 ms rowSize= 14.219 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.068 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anemia, Pernicious C0002892
Definition (1)
Megaloblastic anemia caused by vitamin B-12 deficiency due to impaired absorption. The impaired absorption of vitamin B-12 is secondary to atrophic gastritis and loss of gastric parietal cells.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Anemia, Megaloblastic C0002888
img Vitamin B 12 Deficiency C0042847
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img Anemia, Megaloblastic C0002888
img Nutritional and Metabolic Diseases C0028715img Nutrition Disorders C00287098img Vitamin B 12 Deficiency C0042847
Relationships (48)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 29
diso_​to_​diso : 14


Relationships:
none : 10
associated_​with : 1
classifies : 1
expanded_​form_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 3
mapped_​to : 2
may_​be_​finding_​of_​disease : 1
may_​treat : 26
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO45img Complication Aspects C1171258
DISO_to_DISO38img Complication Aspects C1171258
DISO_to_ANAT22img In Blood C0005768
DISO_to_DISO20img CYANOCOBALAMIN DEFICIENCY C0042847
DISO_to_DISO19img CYANOCOBALAMIN DEFICIENCY C0042847
DISO_to_CHEM17img Vitamin B 12 C0042845
DISO_to_CHEM14img Vitamin B 12 C0042845
DISO_to_ANAT12img In Blood C0005768
DISO_to_DISO11img Stomach Neoplasms C0038356
DISO_to_CHEM9img Intrinsic Factor C0021918
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 Acetatocobalamin C0771561
DISO_to_CHEMmay_treatimg B12 - Hydroxocobalamin prep C0020316
DISO_to_CHEMmay_treatimg CH3-B12 C0065844
DISO_to_CHEMmay_treatimg COBALAMIN CONCENTRATE C0991811
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 0.5 %WV NASAL GEL C0976023
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 1,000 mcg ORAL TABLET C0976004
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 1,000 mcg/mL INJECTION DISPOSABLE SYRINGE (ML) C0976005
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 100 MCG INTRAMUSCULAR INJECTION, SOLUTION C0976011
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 100 mcg ORAL TABLET C0976007
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 10MCG/ML INJ C0976012
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 2,500 mcg SUBLINGUAL TABLET, SUBLINGUAL C0691917
DISO_to_CHEMmay_treatimg CYANOCOBALAMIN 20 mcg/mL INJECTION VIAL (SDV,MDV OR ADDITIVE) (ML) C0976014
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanAMN81693amnion associated transmembrane protein
img OMIM, Score=1000, UMLKSK CUI: C0002892
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
img OMIM, Score=1000, UMLKSK CUI: C0002892
HumanAIRE326autoimmune regulator
img OMIM, Score=1000, UMLKSK CUI: C0002892
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002892Anemia, Pernicious0self