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Details
Link-It Detail - Disease - Apraxias
Debug Stats
  • ### Total Build Time: 35 ms 39.061 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 816 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 1,005 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.391 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 8.009 KB
  • CONCEPT_RELATIONSHIPS gt=15 ms Completed: 15 ms rowSize= 12.617 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 13.593 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Apraxias C0003635
Definition (1)
A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7)
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Psychomotor Disorders C0033922
img Neurobehavioral Manifestations C0525041
Children (3)
img Apraxia, Ideomotor C0234523
img Gait Apraxia C1510417
img Alien Hand Syndrome C2717760
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Psychomotor Disorders C0033922
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Psychomotor Disorders C0033922
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Psychomotor Disorders C0033922
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Neurobehavioral Manifestations C0525041
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Neurobehavioral Manifestations C0525041
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250413img Neurobehavioral Manifestations C0525041
Relationships (45)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 2
diso_​to_​diso : 34
diso_​to_​phen : 2
diso_​to_​phys : 4


Relationships:
none : 26
isa : 16
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO49img Complication Aspects C1171258
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_DISO32img DEFECT SPEECH (NOS) C0037822
DISO_to_DISO30img Complication Aspects C1171258
DISO_to_PHEN29img genetic aspects C0017399
DISO_to_DISO23img Cerebrovascular accident C0038454
DISO_to_DISO18img A-78 DISORDERS OF EYE MOVEMENTS C0028850
DISO_to_ANAT17img Brain C0006104
DISO_to_ANAT15img Brain C0006104
DISO_to_DISO15img Cerebrovascular accident C0038454
DISO_to_PHYS14img Performance, Psychomotor C0033923
DISO_to_DISO13img ARTICULATION DIS C0003910
DISO_to_DISO13img Ataxia C0004134
DISO_to_CHEM12img Binding Protein, DNA C0012940
DISO_to_CHEM12img Nuclear Proteins C0028589
DISO_to_DISO11img Ataxia C0004134
DISO_to_PHYS11img Motor Skill C0026612
DISO_to_DISO10img A-78 DISORDERS OF EYE MOVEMENTS C0028850
DISO_to_DISO10img A60-A63 APHASIAS C0003537
DISO_to_DISO10img Neurodegenerative Diseases C0524851
DISO_to_DISO10img Parkinson Disease C0030567
DISO_to_PHYS10img Functional Laterality C1720777
DISO_to_ANAT9img Eyelid structure C0015426
DISO_to_DISO9img ARTICULATION DIS C0003910
DISO_to_DISO9img Blepharospasm C0005747
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanNHLRC1378884NHL repeat containing 1
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanFOXP293986forkhead box P2
img OMIM, Score=833, UMLKSK CUI: C0003635
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanTREM254209triggering receptor expressed on myeloid cells 2
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
img OMIM, Score=833, UMLKSK CUI: C0003635
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanTBP6908TATA box binding protein
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanCDKL56792cyclin-dependent kinase-like 5
INFERRED, Score=800, UMLKSK CUI: C0003635
HumanPSEN15663presenilin 1
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanPOLG5428polymerase (DNA directed), gamma
img GENERIF, Score=1000, Pubmed Id: 18546343, UMLKSK CUI: C0003635
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED, Score=800, UMLKSK CUI: C0003635
HumanGRN2896granulin
img OMIM, Score=1000, UMLKSK CUI: C0003635
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0003635
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0003635Apraxias0self