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Details
Link-It Detail - Disease - ANEMIA MICROCYTIC
Debug Stats
  • ### Total Build Time: 65 ms 12.177 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=43 ms Completed: 43 ms rowSize= 6.605 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 4.025 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
ANEMIA MICROCYTIC C0085576
Relationships (12)

Relation Types:
diso_​to_​anat : 3
diso_​to_​diso : 9


Relationships:
alias_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 5
manifestation_​of : 3
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
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_DISOalias_ofimg ANEMIA MICROCYTIC C0085576
DISO_to_DISOisaimg Anemia, Iron-Deficiency C0162316
DISO_to_DISOmanifestation_ofimg Anemia, unresponsive to oral iron and only partially responsive to parenteral iron LABORATORY STUDIES : Inappropriately normal or increased plasma hepcidin C3150118
DISO_to_DISOmanifestation_ofimg Caused by mutation in the transmembrane protease, serine 6 gene (TMPRSS6, 609862.0001) C2673912
DISO_to_DISOisaimg Congenital transferrin deficiency C0398541
DISO_to_DISOisaimg Erythroblastosis, Fetal C0014761
DISO_to_DISOmanifestation_ofimg Iron malabsorption C0581365
DISO_to_DISOisaimg Microcytic hypochromic anemia (disorder) C0271901
DISO_to_DISOisaimg Microcytic normochromic anaemia C0271902
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
img OMIM, Score=882, UMLKSK CUI: C0085576
HumanPUS180324pseudouridylate synthase 1
img OMIM, Score=1000, UMLKSK CUI: C0085576
HumanGLRX551218glutaredoxin 5
img GENERIF, Score=1000, Pubmed Id: 17485548, UMLKSK CUI: C0085576
HumanSMPD16609sphingomyelin phosphodiesterase 1, acid lysosomal
img OMIM, Score=1000, UMLKSK CUI: C0085576
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0085576ANEMIA MICROCYTIC0self