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Details
Link-It Detail - Disease - Photophobia
Debug Stats
  • ### Total Build Time: 64 ms 42.657 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 320 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 224 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.061 KB
  • CONCEPT_RELATIONSHIPS gt=47 ms Completed: 47 ms rowSize= 12.857 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 23.309 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Photophobia C0085636
Definition (1)
A condition in which the eyes are more sensitive than normal to light.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Vision Disorders C0042790
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Vision Disorders C0042790
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Vision Disorders C0042790
img Eye Diseases C0015397img Vision Disorders C00427903img Vision Disorders C0042790
Relationships (48)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 30
diso_​to_​diso : 14
diso_​to_​phen : 3


Relationships:
none : 17
mapped_​to : 1
may_​treat : 29
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO11img Migraine Disorders C0149931
DISO_to_DISO8img Alopecia C0002170
DISO_to_PHEN8img genetic aspects C0017399
DISO_to_DISO7img Alopecia C0002170
DISO_to_DISO7img Complication Aspects C1171258
DISO_to_DISO7img Ichthyosis C0020757
DISO_to_DISO7img chemically induced C0007994
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_DISO6img Ichthyoses C0020757
DISO_to_DISO6img Migraine Disorders C0149931
DISO_to_PHEN6img Light C0023693
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_ANAT4img Visual Cortex C0042817
DISO_to_CHEM4img Metalloendopeptidases C1442934
DISO_to_DISO4img Blepharospasm C0005747
DISO_to_DISO4img chemically induced C0007994
DISO_to_CHEMmay_treatimg 1 ML Ketorolac Tromethamine 15 MG/ML Prefilled Syringe C1815885
DISO_to_CHEMmay_treatimg 1 ML Ketorolac Tromethamine 30 MG/ML Prefilled Syringe C1815886
DISO_to_CHEMmay_treatimg 12 HR diclofenac epolamine 15 MG/HR Transdermal Patch C1960406
DISO_to_CHEMmay_treatimg 1H-Pyrrolizine-1-carboxylic acid, 5-benzoyl-2,3-dihydro, (+/-)-, compound with 2-amino-2-(hydroxymethyl)-1,3-propanediol(1:1) C0064326
DISO_to_CHEMmay_treatimg 2 ML Ketorolac Tromethamine 30 MG/ML Prefilled Syringe C0978051
DISO_to_CHEMmay_treatimg 2-((2,6-Dichlorophenyl)amino)-benzeneacetic Acid, Monopotassium Salt C0282131
DISO_to_CHEMmay_treatimg 2-[(2,6-Dichlorophenyl)amino]benzeneacetic Acid C0012091
DISO_to_CHEMmay_treatimg 2-[(2,6-Dichlorophenyl)amino]benzeneacetic Acid Monosodium Salt C0700583
DISO_to_CHEMmay_treatimg 24 HR Diclofenac Sodium 100 MG Extended Release Tablet C0976341
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanMCOLN157192mucolipin 1
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanCNGB354714cyclic nucleotide gated channel beta 3
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanGJB610804gap junction protein, beta 6, 30kDa
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanNR2E310002nuclear receptor subfamily 2, group E, member 3
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanTP638626tumor protein p63
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanXPA7507xeroderma pigmentosum, complementation group A
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanTYR7299tyrosinase
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanTNF7124tumor necrosis factor
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanTGFBI7045transforming growth factor, beta-induced, 68kDa
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanST146768suppression of tumorigenicity 14 (colon carcinoma)
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanSCN1A6323sodium channel, voltage-gated, type I, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanRPE656121retinal pigment epithelium-specific protein 65kDa
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanRPGR6103retinitis pigmentosa GTPase regulator
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanPOLH5429polymerase (DNA directed), eta
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanMITF4286microphthalmia-associated transcription factor
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanCHST64166carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanMAPT4137microtubule-associated protein tau
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanTACSTD24070tumor-associated calcium signal transducer 2
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanHLA-DRB13123
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanGUCY2D3000guanylate cyclase 2D, membrane (retina-specific)
img OMIM, Score=1000, UMLKSK CUI: C0085636
HumanGUCA1A2978guanylate cyclase activator 1A (retina)
img OMIM, Score=1000, UMLKSK CUI: C0085636
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0085636Photophobia0self