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Details
Link-It Detail - Disease - Rare Diseases
Debug Stats
  • ### Total Build Time: 19 ms 16.754 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 367 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 315 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=4 ms Completed: 4 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=1 ms Completed: 1 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.528 KB
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 12.608 KB
  • CONCEPT_GENES gt=0 Completed: 0 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (2)
Rare Diseases C0678236
Disease, Rare
Definition (1)
A large group of diseases which are characterized by a low prevalence in the population. They frequently are associated with problems in diagnosis and treatment.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Disease Attributes C0752357
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Disease Attributes C0752357
Relationships (44)

Relation Types:
diso_​to_​chem : 2
diso_​to_​diso : 37
diso_​to_​gene : 1
diso_​to_​phen : 3
diso_​to_​phys : 1


Relationships:
none : 40
isa : 2
mapped_​to : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN103img genetic aspects C0017399
DISO_to_PHEN41img genetic aspects C0017399
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_DISO20img Neoplasms C0027651
DISO_to_DISO18img Disease, Inborn Genetic C0950123
DISO_to_DISO14img Disease, Hereditary Eye C0015398
DISO_to_DISO14img Retinal Diseases C0035309
DISO_to_DISO10img Lung Diseases C0024115
DISO_to_DISO8img Lymphangioleiomyomatosis C0751674
DISO_to_DISO8img Neoplasms C0027651
DISO_to_DISO8img Nervous System Diseases C0027765
DISO_to_CHEM7img Pharmaceutical Preparations C0013227
DISO_to_DISO7img Complication Aspects C1171258
DISO_to_DISO7img Inborn Errors of Metabolism C0025521
DISO_to_DISO7img Pancreatic Neoplasm C0030297
DISO_to_DISO7img Sarcoma C1261473
DISO_to_DISO6img AUTOIMMUNE DIS C0004364
DISO_to_DISO6img Adenocarcinoma C0001418
DISO_to_DISO6img Dermatologic disorders C0037274
DISO_to_DISO6img Disease, Inborn Genetic C0950123
DISO_to_DISO6img Lung Diseases C0024115
DISO_to_DISO5img Abnormalities, Multiple C0000772
DISO_to_DISO5img DISORDERS OF LYSOSOMAL ENZYMES C0085078
DISO_to_DISO5img Gaucher Disease C0017205
DISO_to_DISO5img Heart Neoplasm C0018809
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0678236Rare Diseases0self