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Details
Link-It Detail - Disease - Progressive Muscular Atrophy
Debug Stats
  • ### Total Build Time: 12 ms 8.187 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 340 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=2 ms Completed: 2 ms rowSize= 4.697 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 1.579 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 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)
A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation.
Relationships (8)

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


Relationships:
classifies : 2
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 2
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_DISOexpanded_form_ofimg 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