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Details
Link-It Detail - Disease - Gait Apraxia
Debug Stats
  • ### Total Build Time: 90 ms 21.845 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 410 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=22 ms Completed: 22 ms rowSize= 253 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 988 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 10.494 KB
  • CONCEPT_RELATIONSHIPS gt=22 ms Completed: 22 ms rowSize= 6.079 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 2.163 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gait Apraxia C1510417
Definition (1)
Impaired ambulation not attributed to sensory impairment or motor weakness. FRONTAL LOBE disorders; BASAL GANGLIA DISEASES (e.g., PARKINSONIAN DISORDERS); DEMENTIA, MULTI-INFARCT; ALZHEIMER DISEASE; and other conditions may be associated with gait apraxia.
Semantic Types (2)
Mental or Behavioral Dysfunction (T048)
Sign or Symptom (T184)
Parents (2)
img Gait Disorders, Neurologic C0751830
img Apraxias C0003635
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Gait Disorders, Neurologic C0751830
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Gait Disorders, Neurologic C0751830
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250415img Apraxias C0003635
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370887img Apraxias C0003635
img Nervous System Diseases C0027765img Neurologic Manifestations C00278546img Apraxias C0003635
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Apraxias C0003635
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Apraxias C0003635
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Apraxias C0003635
Relationships (13)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 9
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 11
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO8img Parkinson Disease C0030567
DISO_to_DISO4img Gait C0016928
DISO_to_ANAT2img Acetabulum C0000962
DISO_to_ANAT2img Brain C0006104
DISO_to_DISO2img COMPL POSTOP C0032787
DISO_to_DISO2img Complication Aspects C1171258
DISO_to_DISO2img Gait C0016928
DISO_to_DISO2img Parkinson Disease C0030567
DISO_to_DISO2img Schizophrenia C0036341
DISO_to_PHEN2img Prosthesis Failure C0033586
DISO_to_PHYS2img Balance, Postural C1256755
DISO_to_DISOmapped_toimg Difficulty walking C0311394
DISO_to_DISOpermuted_term_ofimg Gait Apraxia C1510417
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanCDKL56792cyclin-dependent kinase-like 5
img OMIM, Score=1000, UMLKSK CUI: C1510417
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img OMIM, Score=1000, UMLKSK CUI: C1510417
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1510417Gait Apraxia0self