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Details
Link-It Detail - Disease - Horner Syndrome
Debug Stats
  • ### Total Build Time: 139 ms 24.306 KB
  • CONCEPT_NAME gt=17 ms Completed: 17 ms rowSize= 393 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 534 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 993 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 5.332 KB
  • CONCEPT_RELATIONSHIPS gt=91 ms Completed: 91 ms rowSize= 12.744 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 2.986 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (2)
Horner Syndrome C0019937
Ocular-Ophthalmoplegia, Sympathetic
Definition (1)
syndrome associated with defective sympathetic innervation to one side of the face, including the eye; clinical features include miosis, mild blepharoptosis, and hemifacial anhidrosis (decreased sweating); lesions of the brain stem, cervical spinal cord, first thoracic nerve root, apex of the lung, carotid artery, cavernous sinus, and apex of the orbit may cause this condition.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Autonomic Nervous System Diseases C1145628
img Miosis C0026205
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Autonomic Nervous System Diseases C11456283img Autonomic Nervous System Diseases C1145628
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Miosis C0026205
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Miosis C0026205
img Eye Diseases C0015397img Pupil Disorders C00341244img Miosis C0026205
Relationships (31)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 5
diso_​to_​diso : 21


Relationships:
none : 27
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
mapped_​to : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO38img Complication Aspects C1171258
DISO_to_DISO27img Complication Aspects C1171258
DISO_to_DISO21img Carotid Artery, Internal, Dissection C0751815
DISO_to_CHEM16img 1H-Imidazol-2-amine, N-(2,6-dichlorophenyl)-4,5-dihydro- C0009014
DISO_to_CHEM16img Clonidine C0009014
DISO_to_DISO13img Carotid Artery Dissection, Internal C0751815
DISO_to_DISO13img chemically induced C0007994
DISO_to_DISO10img COMPL POSTOP C0032787
DISO_to_ANAT9img Carotid Artery, Internal C0007276
DISO_to_CHEM9img 1H-Imidazol-2-amine, N-(2,6-dichlorophenyl)-4,5-dihydro- C0009014
DISO_to_CHEM9img Adrenergic alpha-Agonists C0001640
DISO_to_CHEM8img Anesthetics, Local C0002934
DISO_to_DISO7img Head and Neck Neoplasms C0018671
DISO_to_DISO6img Autonomic Nervous System Diseases C1145628
DISO_to_DISO6img Blepharoptosis C0005745
DISO_to_DISO6img Head and Neck Neoplasms C0018671
DISO_to_DISO6img Neuroblastoma C0027819
DISO_to_ANAT5img Carotid Artery, Internal C0007276
DISO_to_ANAT5img Ganglia, Sympathetic C0017071
DISO_to_DISO5img Abducens Nerve Diseases C0271355
DISO_to_DISO5img Anisocoria C0003079
DISO_to_DISO5img Autonomic Nervous System Diseases C1145628
DISO_to_DISO5img Brachial Plexus Neuropathies C0700251
DISO_to_DISO5img Carotid Artery Diseases C0007273
DISO_to_DISO5img Flushing C0016382
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanKIF1B23095kinesin family member 1B
img OMIM, Score=1000, UMLKSK CUI: C0019937
HumanPHOX2B8929paired-like homeobox 2b
img OMIM, Score=1000, UMLKSK CUI: C0019937
HumanNME14830NME/NM23 nucleoside diphosphate kinase 1
img OMIM, Score=1000, UMLKSK CUI: C0019937
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0019937Horner Syndrome0self