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Details
Link-It Detail - Disease - Cerebral Palsy
Debug Stats
  • ### Total Build Time: 55 ms 33.204 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 363 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 557 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.522 KB
  • CONCEPT_RELATIONSHIPS gt=35 ms Completed: 35 ms rowSize= 13.512 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 15.586 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cerebral Palsy C0007789
Definition (1)
A group of disorders affecting the development of movement and posture, often accompanied by disturbances of sensation, perception, cognition, and behavior. It results from damage to the fetal or infant brain.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Brain Damage, Chronic C0006109
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Brain Damage, Chronic C0006109
Relationships (122)

Relation Types:
diso_​to_​anat : 21
diso_​to_​chem : 26
diso_​to_​diso : 59
diso_​to_​phen : 2
diso_​to_​phys : 14


Relationships:
none : 87
is_​associated_​anatomic_​site_​of : 2
isa : 12
mapped_​to : 8
may_​treat : 13
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO715img Complication Aspects C1171258
DISO_to_DISO472img Complication Aspects C1171258
DISO_to_DISO159img Gait C0016928
DISO_to_CHEM142img Botulinum Toxin Type A C0006050
DISO_to_CHEM142img Botulinum Toxins, Type A C0006050
DISO_to_PHYS134img Motor Skill C0026612
DISO_to_ANAT133img Muscle, Skeletal C0242692
DISO_to_DISO130img Gait Disorders, Neurologic C0751830
DISO_to_DISO129img Hemiplegia C0018991
DISO_to_DISO110img Muscle Spasticity C0026838
DISO_to_CHEM104img Agents, Neuromuscular C0027865
DISO_to_CHEM100img Botulinum Toxin Type A C0006050
DISO_to_DISO94img Developmental Disabilities C0008073
DISO_to_ANAT84img Muscle, Skeletal C0242692
DISO_to_CHEM84img Agents, Neuromuscular C0027865
DISO_to_DISO79img Muscle Spasticity C0026838
DISO_to_DISO76img Gait C0016928
DISO_to_DISO69img Hip Dislocation C0019554
DISO_to_ANAT61img Upper Extremity C1140618
DISO_to_PHYS59img Body position C1262869
DISO_to_PHYS57img Movement C0026649
DISO_to_DISO56img Motor Skills Disorders C0026613
DISO_to_PHYS56img Range of Motion, Articular C0080078
DISO_to_DISO54img HEMIPLEGIA C0018991
DISO_to_PHYS51img CHILDHOOD DEVELOPMENT C0008071
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
img OMIM, Score=1000, UMLKSK CUI: C0007789
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 18391842, UMLKSK CUI: C0007789
HumanPLP15354proteolipid protein 1
img GENERIF, Score=1000, Pubmed Id: 18437021, UMLKSK CUI: C0007789
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img GAD, Score=1000, Pubmed Id: 15718364, UMLKSK CUI: C0007789
HumanMBL24153mannose-binding lectin (protein C) 2, soluble
img GENERIF, Score=1000, Pubmed Id: 18455525, UMLKSK CUI: C0007789
HumanLTA4049lymphotoxin alpha
img GAD, Score=1000, Pubmed Id: 15718364, UMLKSK CUI: C0007789
HumanIL183606interleukin 18 (interferon-gamma-inducing factor)
img GENERIF, Score=1000, Pubmed Id: 11895335, UMLKSK CUI: C0007789
HumanIGFBP33486insulin-like growth factor binding protein 3
img GENERIF, Score=1000, Pubmed Id: 17912004, UMLKSK CUI: C0007789
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
img GENERIF, Score=1000, Pubmed Id: 17912004, UMLKSK CUI: C0007789
HumanGSR2936glutathione reductase
img GENERIF, Score=1000, Pubmed Id: 15978628, UMLKSK CUI: C0007789
HumanGPX42879glutathione peroxidase 4
img GENERIF, Score=1000, Pubmed Id: 15978628, UMLKSK CUI: C0007789
HumanF72155coagulation factor VII (serum prothrombin conversion accelerator)
img GAD, Score=1000, Pubmed Id: 15718364, UMLKSK CUI: C0007789
HumanF52153coagulation factor V (proaccelerin, labile factor)
img GENERIF, Score=734, Pubmed Id: 16359589, UMLKSK CUI: C0007789
HumanAPOE348apolipoprotein E
img GENERIF, Score=1000, Pubmed Id: 18810496, UMLKSK CUI: C0007789
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0007789Cerebral Palsy0self