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Details
Link-It Detail - Disease - Paroxysmal nocturnal hemoglobinuria
Debug Stats
  • ### Total Build Time: 19 ms 23.009 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 466 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=7 ms Completed: 7 ms rowSize= 4.537 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 16.418 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Paroxysmal nocturnal hemoglobinuria C0024790
Definition (1)
A rare disorder in which red blood cells are easily destroyed by certain immune system proteins. Symptoms include blood clots, and red or brownish urine in the morning. Aplastic anemia (decreased production of blood cells) may lead to PNH, and people with PNH are at increased risk of acute myelogenous leukemia.
Relationships (6)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 2


Relationships:
clinically_​similar : 2
gene_​product_​malfunction_​associated_​with_​disease : 1
is_​associated_​anatomic_​site_​of : 1
is_​normal_​cell_​origin_​of_​disease : 1
is_​normal_​tissue_​origin_​of_​disease : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg HEMOLYMPHORETICULAR TISSUE C1512398
DISO_to_ANATis_associated_anatomic_site_ofimg Hematopoietic and Lymphatic System C1512394
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Hematopoietic and Lymphoid Cell C1512385
DISO_to_CHEMgene_product_malfunction_associated_with_diseaseimg Phosphatidylinositol N-Acetylglucosaminyltransferase Subunit A C3272445
DISO_to_DISOclinically_similarimg PAROXYSMAL NOCTURNAL HEMOGLOBINURIA INVOLVING KIDNEYS C0519046
DISO_to_DISOclinically_similarimg Paroxysmal nocturnal hemoglobinuria C0024790
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanPECI10455
img GENERIF, Score=694, Pubmed Id: 15217832, UMLKSK CUI: C0024790
HumanWT17490Wilms tumor 1
img GENERIF, Score=1000, Pubmed Id: 12070003, UMLKSK CUI: C0024790
HumanTERC7012telomerase RNA component
img GENERIF, Score=1000, Pubmed Id: 12676774, UMLKSK CUI: C0024790
HumanPRNP5621prion protein
img GENERIF, Score=1000, Pubmed Id: 12070046, UMLKSK CUI: C0024790
HumanPLAU5328plasminogen activator, urokinase
img GENERIF, Score=1000, Pubmed Id: 12041678, UMLKSK CUI: C0024790
HumanPIGA5277phosphatidylinositol glycan anchor biosynthesis, class A
img GENERIF, Score=1000, Pubmed Id: 16923549, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 12037021, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 19013003, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 12130519, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 12411324, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 12424196, UMLKSK CUI: C0024790
img GENERIF, Score=1000, Pubmed Id: 17823237, UMLKSK CUI: C0024790
HumanHLA-DRB13123
img GENERIF, Score=1000, Pubmed Id: 12070003, UMLKSK CUI: C0024790
HumanHLA-DQB13119
img GENERIF, Score=1000, Pubmed Id: 12070003, UMLKSK CUI: C0024790
HumanCD551604CD55 molecule, decay accelerating factor for complement (Cromer blood group)
img GENERIF, Score=1000, Pubmed Id: 18158579, UMLKSK CUI: C0024790
img GENERIF, Score=756, Pubmed Id: 16908271, UMLKSK CUI: C0024790
HumanCD59966CD59 molecule, complement regulatory protein
img GENERIF, Score=1000, Pubmed Id: 18158579, UMLKSK CUI: C0024790
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0024790Paroxysmal nocturnal hemoglobinuria0self