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Details
Link-It Detail - Disease - Gait Disorders, Neurologic
Debug Stats
  • ### Total Build Time: 283 ms 36.270 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 405 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 482 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=4 ms Completed: 4 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 979 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.819 KB
  • CONCEPT_RELATIONSHIPS gt=201 ms Completed: 201 ms rowSize= 12.619 KB
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 17.090 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Gait Disorders, Neurologic C0751830
AMBULATION DIS NEUROLOGIC
Definition (1)
Gait abnormalities that are a manifestation of nervous system dysfunction. These conditions may be caused by a wide variety of disorders which affect motor control, sensory feedback, and muscle strength including: CENTRAL NERVOUS SYSTEM DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; or MUSCULAR DISEASES.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Neurologic Manifestations C0027854
Children (2)
img Gait Apraxia C1510417
img Gait Ataxia C0751837
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Neurologic Manifestations C0027854
img Nervous System Diseases C0027765img Neurologic Manifestations C00278543img Neurologic Manifestations C0027854
Relationships (71)

Relation Types:
diso_​to_​anat : 14
diso_​to_​chem : 4
diso_​to_​diso : 40
diso_​to_​phen : 2
diso_​to_​phys : 11


Relationships:
none : 68
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO250img Gait C0016928
DISO_to_DISO220img Stroke C0038454
DISO_to_DISO212img Parkinson Disease C0030567
DISO_to_DISO130img Cerebral Palsy C0007789
DISO_to_PHYS100img Postural Balance C1256755
DISO_to_ANAT82img Muscle, Skeletal C0242692
DISO_to_DISO67img Gait C0016928
DISO_to_DISO67img Paresis C0030552
DISO_to_DISO63img Cerebrovascular accident C0038454
DISO_to_DISO63img Complication Aspects C1171258
DISO_to_DISO58img Spinal Cord Injuries C0037929
DISO_to_DISO49img ACCIDENTAL FALLS C0000921
DISO_to_DISO48img Cerebral Palsy C0007789
DISO_to_DISO45img Parkinson Disease C0030567
DISO_to_ANAT41img Leg C1140621
DISO_to_ANAT40img Foot C0016504
DISO_to_ANAT40img Muscle, Skeletal C0242692
DISO_to_DISO40img Spinal Cord Injuries C0037929
DISO_to_ANAT39img Knee Joint C0022745
DISO_to_DISO37img Cognition Disorders C0009241
DISO_to_DISO37img Hemiplegia C0018991
DISO_to_ANAT34img Ankle joint structure C0003087
DISO_to_DISO34img Multiple Sclerosis C0026769
DISO_to_DISO32img Recovery of Function C0599766
DISO_to_DISO32img chemically induced C0007994
Genes (28)

Species:
human : 28
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanC10orf256652chromosome 10 open reading frame 2
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanAPTX54840aprataxin
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPDP154704pyruvate dehyrogenase phosphatase catalytic subunit 1
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanSACS26278spastic ataxia of Charlevoix-Saguenay (sacsin)
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPLEKHG425894pleckstrin homology domain containing, family G (with RhoGef domain) member 4
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanATXN1025814ataxin 10
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanSETX23064senataxin
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanCUL4B8450cullin 4B
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanTBP6908TATA box binding protein
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanCDKL56792cyclin-dependent kinase-like 5
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanSPTBN26712spectrin, beta, non-erythrocytic 2
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanSPG76687spastic paraplegia 7 (pure and complicated autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPSAP5660prosaposin
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPRNP5621prion protein
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPRKCG5582protein kinase C, gamma
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPOLG5428polymerase (DNA directed), gamma
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanPMP225376peripheral myelin protein 22
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanOPHN14983oligophrenin 1
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanMPZ4359myelin protein zero
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanKCNC33748potassium voltage-gated channel, Shaw-related subfamily, member 3
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanITPR13708inositol 1,4,5-trisphosphate receptor, type 1
INFERRED, Score=800, UMLKSK CUI: C0751830
HumanHLA-DQB13119
INFERRED, Score=800, UMLKSK CUI: C0751830
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751830Gait Disorders, Neurologic0self