Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Disease - Anemia, Hemolytic
Debug Stats
  • ### Total Build Time: 94 ms 43.567 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 322 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=0 Completed: 0 ms rowSize= 542 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 2.272 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.502 KB
  • CONCEPT_RELATIONSHIPS gt=50 ms Completed: 50 ms rowSize= 15.278 KB
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 21.938 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anemia, Hemolytic C0002878
ANAEMIA HAEMOLYTIC
Definition (1)
Anemia resulting from the premature destruction of the peripheral blood red cells. It may be congenital or it may be caused by infections, medications, or malignancies.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Anemia C0002871
Children (5)
img Hemoglobinuria, Paroxysmal C0019050
img Hemolytic-Uremic Syndrome C0019061
img Favism C0015702
img Anemia, Hemolytic, Autoimmune C0002880
img Anemia, Hemolytic, Congenital C0002881
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Anemia C0002871
Relationships (115)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 56
diso_​to_​diso : 47
diso_​to_​gene : 2
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 63
gene_​associated_​with_​disease : 2
gene_​product_​malfunction_​associated_​with_​disease : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 10
mapped_​to : 6
may_​prevent : 17
may_​treat : 11
parent_​is_​cdrh : 1
use : 1
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO115img chemically induced C0007994
DISO_to_DISO104img chemically induced C0007994
DISO_to_ANAT73img In Blood C0005768
DISO_to_DISO59img Complication Aspects C1171258
DISO_to_ANAT58img In Blood C0005768
DISO_to_DISO55img Complication Aspects C1171258
DISO_to_PHEN55img genetic aspects C0017399
DISO_to_PHEN35img genetic aspects C0017399
DISO_to_DISO25img Thrombocytopenia C0040034
DISO_to_DISO22img Hemolysis C0019054
DISO_to_ANAT20img Erythrocytes C0014792
DISO_to_DISO20img Hemolysis C0019054
DISO_to_DISO19img Glucosephosphate Dehydrogenase Deficiency C0017758
DISO_to_DISO18img Glucosephosphate Dehydrogenase Deficiency C0017758
DISO_to_DISO18img Thrombocytopenia C0040034
DISO_to_CHEM16img Antibodies, Monoclonal C0003250
DISO_to_CHEM15img Ribavirin C0035525
DISO_to_CHEM13img Anti-Bacterial Agents C0279516
DISO_to_CHEM13img Antiviral Agents C0003451
DISO_to_DISO13img COMPL POSTOP C0032787
DISO_to_DISO13img Chronic Hepatitis C C0524910
DISO_to_ANAT12img ABO Blood-Group System C0000778
DISO_to_CHEM12img Anti-Bacterial Agents C0279516
DISO_to_DISO12img Blood Group Incompatibilities C0005806
DISO_to_DISO12img Purpura, Thrombotic Thrombocytopenic C0034155
Genes (147)

Species:
human : 147
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
img OMIM, Score=1000, UMLKSK CUI: C0002878
img GENERIF, Score=1000, Pubmed Id: 12192084, UMLKSK CUI: C0002878
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanHBA@83587
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanCFHR581494complement factor H-related 5
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanSLEB364695systemic lupus erythematosus susceptibility 3
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanHBB@64162
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanHAMP57817hepcidin antimicrobial peptide
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanBANK155024B-cell scaffold protein with ankyrin repeats 1
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanA4GALT53947alpha 1,4-galactosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanBCL11A53335B-cell CLL/lymphoma 11A (zinc finger protein)
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanAHSP51327alpha hemoglobin stabilizing protein
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanNT5C3512515'-nucleotidase, cytosolic III
img OMIM, Score=1000, UMLKSK CUI: C0002878
img GENERIF, Score=1000, Pubmed Id: 18499901, UMLKSK CUI: C0002878
HumanFOXP350943forkhead box P3
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanPALLD23022palladin, cytoskeletal associated protein
INFERRED, Score=800, UMLKSK CUI: C0002878
HumanTREX111277three prime repair exonuclease 1
img OMIM, Score=1000, UMLKSK CUI: C0002878
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
INFERRED, Score=800, UMLKSK CUI: C0002878
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002878Anemia, Hemolytic0self