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Details
Link-It Detail - Disease - Neurologic Manifestations
Debug Stats
  • ### Total Build Time: 88 ms 43.628 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 399 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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= 176 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 995 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 9.916 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.804 KB
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 9.234 KB
  • CONCEPT_GENES gt=68 ms Completed: 68 ms rowSize= 18.730 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Neurologic Manifestations C0027854
MANIFESTATIONS NEUROL
Definition (1)
Clinical signs and symptoms caused by nervous system injury or dysfunction.
Semantic Types (1)
Finding (T033)
Parents (2)
img Signs and Symptoms C0037088
img Nervous System Diseases C0027765
Children (23)
img Paresis C0030552
img Dyskinesias C0013384
img Seizures C0036572
img Reflex, Abnormal C0034933
img Neuromuscular Manifestations C0752252
img Decerebrate State C0011103
img Psychophysiologic Disorders C0033931
img Sleep Disorders C0851578
img Pain C0030193
img Gait Disorders, Neurologic C0751830
img Sensation Disorders C0036659
img Voice Disorders C0042940
img Orthostatic Intolerance C1535893
img Susac Syndrome C2717757
img Cerebrospinal Fluid Otorrhea C0007814
img Cerebrospinal Fluid Rhinorrhea C0007815
img Neurobehavioral Manifestations C0525041
img Vertigo C0042571
img Neurogenic Inflammation C0600467
img Urinary Bladder, Neurogenic C0005697
img Meningism C0025287
img Paralysis C0522224
img Pupil Disorders C0034124
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370883img Signs and Symptoms C0037088
img Nervous System Diseases C0027765img Signs and Symptoms C00370882img Nervous System Diseases C0027765
Relationships (21)

Relation Types:
diso_​to_​chem : 19
diso_​to_​diso : 2


Relationships:
may_​treat : 19
permuted_​term_​of : 1
use : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMmay_treatimg (6alpha,11beta)-11,17,21-Trihydroxy-6-methylpregna-1,4-diene-3,20-dione C0025815
DISO_to_CHEMmay_treatimg 11beta,17,21-Trihydroxy-6alpha-methylpregna-1,4-diene-3,20-dione 21-Acetate C0600901
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 16 MG ORAL TABLET C1123025
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 2 MG ORAL TABLET C0689573
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 24 MG Oral (systemic) tablet C0689574
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 32 MG ORAL TABLET C0689575
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 40 MG INTRALESIONAL INJECTION, SUSPENSION C1161515
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE 8 MG ORAL TABLET C0689577
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE ACET 40MG/BTL RTL PWD C0978589
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE ACETATE 0.25 % TOPICAL OINTMENT(GM) C0784786
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE ACETATE 1 % TOPICAL OINTMENT(GM) C0784787
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE ACETATE 20 MG INTRA-ARTICULAR INJECTION, SUSPENSION C0775279
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE HEMISUCC 40MG VIAL (SDV,MDV OR ADDITIVE) (EA) C0978593
DISO_to_CHEMmay_treatimg METHYLPREDNISOLONE NA SUCC 2GM/VIL INJ C0978592
DISO_to_CHEMmay_treatimg Methylprednisolone 4 MG Oral Tablet C0873969
DISO_to_CHEMmay_treatimg Methylprednisolone 4 mg Oral Tablet includes 21 Day Pack C2727935
DISO_to_CHEMmay_treatimg Methylprednisolone 62.5 MG/ML Injectable Solution C0981582
DISO_to_CHEMmay_treatimg Methylprednisolone 80 MG/ML Injectable Suspension C0775281
DISO_to_CHEMmay_treatimg Methylprednisolone Sodium Succinate C0700546
DISO_to_DISOuseimg Fasciculation C0015644
DISO_to_DISOpermuted_term_ofimg MANIFESTATIONS NEUROL C0027854
Genes (1511)

Species:
human : 1511
Page Size
Current 25
  Page 1 of 61
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDFNB72791116
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanNCRNA00163727699
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanZNF674641339zinc finger protein 674
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanSCZD12619488schizophrenia 12
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDFNB55494148deafness, autosomal recessive 55
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanADHD4450090Attention deficit-hyperactivity disorder, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanADHD3450089Attention deficit-hyperactivity disorder, susceptibility to, 2
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanADHD2450088Attention deficit-hyperactivity disorder, susceptibility to, 2
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanADHD1450087Attention deficit-hyperactivity disorder, susceptibility to, 1
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDFNB45449483deafness, autosomal recessive 45
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDFNA54448962deafness, autosomal dominant 54
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanMIR212406994microRNA 212
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanDYX8406874dyslexia susceptibility 8
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanSCZD11404686Schizophrenia susceptibility locus, chromosome 10q-related
INFERRED, Score=800, UMLKSK CUI: C0027854
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
INFERRED, Score=800, UMLKSK CUI: C0027854
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0027854Neurologic Manifestations0self