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Details
Link-It Detail - Disease - Pupil Disorders
Debug Stats
  • ### Total Build Time: 97 ms 25.811 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 349 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=10 ms Completed: 10 ms rowSize= 991 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.786 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.680 KB
  • CONCEPT_RELATIONSHIPS gt=52 ms Completed: 52 ms rowSize= 12.198 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 5.157 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Pupil Disorders C0034124
Definition (1)
Conditions which affect the structure or function of the pupil of the eye, including disorders of innervation to the pupillary constrictor or dilator muscles, and disorders of pupillary reflexes.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Eye Diseases C0015397
img Neurologic Manifestations C0027854
Children (4)
img Tonic Pupil C0040416
img Miosis C0026205
img Anisocoria C0003079
img Mydriasis C0026961
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C00153972img Eye Diseases C0015397
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 (39)

Relation Types:
diso_​to_​anat : 6
diso_​to_​diso : 31
diso_​to_​phen : 2


Relationships:
none : 22
isa : 11
mapped_​to : 5
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT25img Iris C0022077
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO15img Complication Aspects C1171258
DISO_to_DISO13img Eye Abnormalities C0015393
DISO_to_DISO13img Iris Diseases C0022078
DISO_to_DISO11img Disorder of the optic nerve C0029132
DISO_to_ANAT10img Iris C0022077
DISO_to_DISO10img Glaucoma, Angle-Closure C0017605
DISO_to_ANAT9img Pupil C0034121
DISO_to_ANAT8img Pupil C0034121
DISO_to_DISO8img Glaucoma C0017601
DISO_to_DISO8img Vision Disorders C0042790
DISO_to_PHEN8img genetic aspects C0017399
DISO_to_DISO7img Autonomic Nervous System Diseases C1145628
DISO_to_DISO7img Disease of Iris C0022078
DISO_to_DISO7img Glaucoma, Open-Angle C0017612
DISO_to_DISO7img chemically induced C0007994
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_ANAT6img Anterior Chamber C0003151
DISO_to_ANAT6img Optic Nerve C0029130
DISO_to_DISO6img Abnormalities, Multiple C0000772
DISO_to_DISO6img COMPL POSTOP C0032787
DISO_to_DISOisaimg ANISOCORIA C0003079
DISO_to_DISOisaimg Abn pupil function NOS C0917967
DISO_to_DISOisaimg Adhesion of pupillary membrane C2960545
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanKIF1B23095kinesin family member 1B
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanPHOX2B8929paired-like homeobox 2b
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanPHYH5264phytanoyl-CoA 2-hydroxylase
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanPEX75191peroxisomal biogenesis factor 7
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanSIX64990SIX homeobox 6
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanNME14830NME/NM23 nucleoside diphosphate kinase 1
INFERRED, Score=800, UMLKSK CUI: C0034124
HumanDDC1644dopa decarboxylase (aromatic L-amino acid decarboxylase)
INFERRED, Score=800, UMLKSK CUI: C0034124
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0034124Pupil Disorders0self