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Details
Link-It Detail - Disease - Progressive Muscular Atrophy
Debug Stats
  • ### Total Build Time: 67 ms 8.170 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 351 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=35 ms Completed: 35 ms rowSize= 4.670 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 1.579 KB
  • CONCEPT_XREFS gt=15 ms Completed: 15 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Progressive Muscular Atrophy C0917981
Definition (1)
group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts.
Relationships (8)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 6


Relationships:
classifies : 2
is_​associated_​anatomic_​site_​of : 2
mapped_​to : 1
use : 2
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_associated_anatomic_site_ofimg Central Nervous System C0927232
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_DISOused_forimg A-23 MOTOR NEURON DISEASES C0085084
DISO_to_DISOuseimg HMN (Hereditary Motor Neuropathy) Proximal Type I C0043116
DISO_to_DISOclassifiesimg Other and unspecified hereditary and degenerative nervous conditions C0810267
DISO_to_DISOclassifiesimg Other hereditary and degenerative nervous system conditions C0809991
DISO_to_DISOmapped_toimg Progressive Muscular Atrophy C0917981
DISO_to_DISOuseimg Werdnig Hoffmann paralysis C0599201
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanAR367androgen receptor
img GENERIF, Score=1000, Pubmed Id: 17997416, UMLKSK CUI: C0917981
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0917981Progressive Muscular Atrophy0self