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Details
Link-It Detail - Disease - Anemia, Neonatal
Debug Stats
  • ### Total Build Time: 179 ms 11.320 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 242 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=104 ms Completed: 104 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 985 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 1,001 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 2.827 KB
  • CONCEPT_RELATIONSHIPS gt=33 ms Completed: 33 ms rowSize= 4.590 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anemia, Neonatal C0002891
Definition (1)
The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Infant, Newborn, Diseases C0021290
img Anemia C0002871
Children (2)
img Fetomaternal Transfusion C0015959
img Fetofetal Transfusion C0015958
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212903img Infant, Newborn, Diseases C0021290
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Anemia C0002871
Relationships (9)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 2
diso_​to_​diso : 6


Relationships:
none : 4
isa : 4
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM25img Erythropoietin C0014822
DISO_to_ANAT17img In Blood C0005768
DISO_to_CHEM15img Erythropoietin C0014822
DISO_to_DISO13img Infant, Premature, Diseases C0021295
DISO_to_DISOpermuted_term_ofimg ANAEMIA NEONATAL C0002891
DISO_to_DISOisaimg AOP C0158996
DISO_to_DISOisaimg Kernicterus - due to isoimm. C0270204
DISO_to_DISOisaimg Late anaemia of newborn C0475726
DISO_to_DISOisaimg Physiological anaemia of infancy C0475725
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002891Anemia, Neonatal0self