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Details
Link-It Detail - Disease - Paraplegia
Debug Stats
  • ### Total Build Time: 58 ms 21.229 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 241 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 545 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 560 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.788 KB
  • CONCEPT_RELATIONSHIPS gt=38 ms Completed: 38 ms rowSize= 13.892 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 1.518 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Paraplegia C0030486
EXTREMITY PARALYSIS, LOWER
Definition (1)
complete or partial loss of movement in the lower part of the body, including both legs
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Paralysis C0522224
Children (1)
img Brown-Sequard Syndrome C0242644
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Paralysis C0522224
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Paralysis C0522224
Relationships (99)

Relation Types:
diso_​to_​anat : 18
diso_​to_​chem : 1
diso_​to_​diso : 70
diso_​to_​phen : 2
diso_​to_​phys : 8


Relationships:
none : 79
associated_​with : 1
classifies : 2
clinically_​similar : 1
is_​associated_​anatomic_​site_​of : 1
isa : 5
mapped_​to : 9
parent_​is_​cdrh : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO132img Spinal Cord Injuries C0037929
DISO_to_DISO119img Spinal Cord Injuries C0037929
DISO_to_DISO101img Complication Aspects C1171258
DISO_to_DISO89img Complication Aspects C1171258
DISO_to_PHEN50img genetic aspects C0017399
DISO_to_DISO49img Spinal Cord Ischemia C0752130
DISO_to_DISO45img COMPL POSTOP C0032787
DISO_to_DISO44img Aortic Aneurysm, Thoracic C0162872
DISO_to_ANAT41img Spinal Cord C0037925
DISO_to_DISO35img Aortic Aneurysm, Thoracic C0162872
DISO_to_DISO35img Quadriplegia C0034372
DISO_to_DISO35img Spinal Cord Ischemia C0752130
DISO_to_DISO34img Quadriplegia C0034372
DISO_to_DISO33img Compression of spinal cord C0037926
DISO_to_PHEN32img genetic aspects C0017399
DISO_to_ANAT31img Muscle, Skeletal C0242692
DISO_to_ANAT31img Spinal Cord C0037925
DISO_to_DISO29img Compression of spinal cord C0037926
DISO_to_ANAT27img Bone structure of thoracic vertebra C0039987
DISO_to_DISO27img COMPL POSTOP C0032787
DISO_to_DISO24img Aortic Aneurysm, Abdominal C0162871
DISO_to_ANAT23img Bone structure of thoracic vertebra C0039987
DISO_to_DISO23img Spinal Neoplasms C0037939
DISO_to_ANAT22img Muscle, Skeletal C0242692
DISO_to_DISO21img ANEURYSM, DISSECTING C0002949
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPAST6683spastin
img GENERIF, Score=827, Pubmed Id: 17597328, UMLKSK CUI: C0030486
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030486Paraplegia0self