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Details
Link-It Detail - Disease - Idiopathic Interstitial Pneumonias
Debug Stats
  • ### Total Build Time: 64 ms 17.866 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 481 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=7 ms Completed: 7 ms rowSize= 563 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1,017 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.514 KB
  • CONCEPT_RELATIONSHIPS gt=23 ms Completed: 23 ms rowSize= 7.678 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 4.926 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Idiopathic Interstitial Pneumonias C2350236
Definition (1)
A group of interstitial lung diseases with no known etiology. There are several entities with varying patterns of inflammation and fibrosis. They are classified by their distinct clinical-radiological-pathological features and prognosis. They include IDIOPATHIC PULMONARY FIBROSIS; CRYPTOGENIC ORGANIZING PNEUMONIA; and others.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Lung Diseases, Interstitial C0206062
Children (2)
img Idiopathic Pulmonary Fibrosis C1800706
img Cryptogenic Organizing Pneumonia C0242770
Ancestral Roots
RootRoot Plus OneDepthParent
img Respiratory Tract Diseases C0035242img Lung Diseases C00241154img Lung Diseases, Interstitial C0206062
Relationships (17)

Relation Types:
diso_​to_​anat : 5
diso_​to_​diso : 11
diso_​to_​phen : 1


Relationships:
none : 8
is_​associated_​anatomic_​site_​of : 3
isa : 5
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO15img Complication Aspects C1171258
DISO_to_ANAT8img Lung C0024109
DISO_to_DISO7img Lung Neoplasms C0024121
DISO_to_DISO5img Idiopathic Pulmonary Fibrosis C1800706
DISO_to_DISO5img Lung Diseases, Interstitial C0206062
DISO_to_ANAT4img In Blood C0005768
DISO_to_DISO4img Connective Tissue Diseases C0009782
DISO_to_PHEN4img genetic aspects C0017399
DISO_to_ANATis_associated_anatomic_site_ofimg Chest C0817096
DISO_to_ANATis_associated_anatomic_site_ofimg Lung C0024109
DISO_to_ANATis_associated_anatomic_site_ofimg Respiratory System C0035237
DISO_to_DISOisaimg Acute interstitial pneumonia C1279945
DISO_to_DISOisaimg Desquamative interstitial pneumonia C0238378
DISO_to_DISOpermuted_term_ofimg Idiopathic Interstitial Pneumonias C2350236
DISO_to_DISOisaimg Idiopathic Pulmonary Fibrosis C1800706
DISO_to_DISOisaimg Lymphoid interstitial pneumonia C0264511
DISO_to_DISOisaimg Nonspecific interstitial pneumonia C1290344
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTLR954106toll-like receptor 9
img GENERIF, Score=1000, Pubmed Id: 18633634, UMLKSK CUI: C2350236
HumanCCL186362chemokine (C-C motif) ligand 18 (pulmonary and activation-regulated)
img GENERIF, Score=1000, Pubmed Id: 17469163, UMLKSK CUI: C2350236
HumanCMA11215chymase 1, mast cell
img GENERIF, Score=1000, Pubmed Id: 17334631, UMLKSK CUI: C2350236
HumanAGTR1185angiotensin II receptor, type 1
img GENERIF, Score=1000, Pubmed Id: 18432064, UMLKSK CUI: C2350236
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C2350236Idiopathic Interstitial Pneumonias0self