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Pediatric Disease Annotations & Medicines



   ectropion
  

Disease ID 1553
Disease ectropion
Definition
The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed)
Synonym
ectropion (disorder)
ectropion (m-31318)
ectropion [disease/finding]
ectropion eyelids
ectropion nos
ectropion nos (disorder)
ectropion of eyelid
ectropion of eyelid (disorder)
ectropion, nos
ectropion, unspecified
ectropions
eversion of the eyelid
everted eyelid
everted margin
everted margin (morphologic abnormality)
extropion
eyelashes turned out
eyelid ectropion
eyelid everted
eyelid folded out
eyelid turned out
unspecified ectropion
unspecified ectropion (disorder)
DOID
UMLS
C0013592
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:24)
C0017601  |  glaucoma  |  3
C0020758  |  lamellar ichthyosis  |  2
C0005745  |  ptosis  |  2
C0003076  |  aniridia  |  2
C0037274  |  skin disease  |  1
C0031099  |  periodontitis  |  1
C0162359  |  hypohidrotic ectodermal dysplasia  |  1
C0032027  |  pityriasis rubra pilaris  |  1
C0085113  |  neurofibromatosis  |  1
C0005741  |  blepharitis  |  1
C0020302  |  developmental glaucoma  |  1
C0009763  |  conjunctivitis  |  1
C0409974  |  lupus erythematosus  |  1
C0022568  |  keratitis  |  1
C0020302  |  juvenile glaucoma  |  1
C0013575  |  ectodermal dysplasia  |  1
C0155145  |  chronic conjunctivitis  |  1
C0010495  |  cutis laxa  |  1
C0376358  |  prostate cancer  |  1
C0152226  |  lagophthalmos  |  1
C0007117  |  basal cell carcinoma  |  1
C0152227  |  epiphora  |  1
C0037274  |  skin diseases  |  1
C0235270  |  keratopathy  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:71)
4653  |  MYOC  |  DISEASES
3861  |  KRT14  |  DISEASES
7145  |  TNS1  |  DISEASES
7051  |  TGM1  |  DISEASES
55612  |  FERMT1  |  DISEASES
1723  |  DHODH  |  DISEASES
13  |  AADAC  |  DISEASES
374291  |  NDUFS7  |  DISEASES
3848  |  KRT1  |  DISEASES
29969  |  MDFIC  |  DISEASES
1545  |  CYP1B1  |  DISEASES
23314  |  SATB2  |  DISEASES
10133  |  OPTN  |  DISEASES
80725  |  SRCIN1  |  DISEASES
3858  |  KRT10  |  DISEASES
126410  |  CYP4F22  |  DISEASES
26154  |  ABCA12  |  DISEASES
5295  |  PIK3R1  |  DISEASES
4851  |  NOTCH1  |  DISEASES
204219  |  CERS3  |  DISEASES
760  |  CA2  |  DISEASES
6529  |  SLC6A1  |  DISEASES
5304  |  PIP  |  DISEASES
1409  |  CRYAA  |  DISEASES
121214  |  SDR9C7  |  DISEASES
10999  |  SLC27A4  |  DISEASES
4909  |  NTF4  |  DISEASES
332  |  BIRC5  |  DISEASES
51181  |  DCXR  |  DISEASES
5308  |  PITX2  |  DISEASES
1816  |  DRD5  |  DISEASES
392  |  ARHGAP1  |  DISEASES
348938  |  NIPAL4  |  DISEASES
59344  |  ALOXE3  |  DISEASES
242  |  ALOX12B  |  DISEASES
57381  |  RHOJ  |  DISEASES
923  |  CD6  |  DISEASES
2  |  A2M  |  DISEASES
2303  |  FOXC2  |  DISEASES
1538  |  CYLC1  |  DISEASES
668  |  FOXL2  |  DISEASES
26151  |  NAT9  |  DISEASES
4763  |  NF1  |  DISEASES
147409  |  DSG4  |  DISEASES
4014  |  LOR  |  DISEASES
7390  |  UROS  |  DISEASES
2312  |  FLG  |  DISEASES
4952  |  OCRL  |  DISEASES
26508  |  HEYL  |  DISEASES
7403  |  KDM6A  |  DISEASES
285440  |  CYP4V2  |  DISEASES
5080  |  PAX6  |  DISEASES
2296  |  FOXC1  |  DISEASES
352909  |  DNAAF3  |  DISEASES
285848  |  PNPLA1  |  DISEASES
1365  |  CLDN3  |  DISEASES
643418  |  LIPN  |  DISEASES
22976  |  PAXIP1  |  DISEASES
55777  |  MBD5  |  DISEASES
51099  |  ABHD5  |  DISEASES
3481  |  IGF2  |  DISEASES
1638  |  DCT  |  DISEASES
23705  |  CADM1  |  DISEASES
27151  |  CPAMD8  |  DISEASES
9278  |  ZBTB22  |  DISEASES
117581  |  TWIST2  |  DISEASES
54900  |  LAX1  |  DISEASES
81704  |  DOCK8  |  DISEASES
134430  |  WDR36  |  DISEASES
2053  |  EPHX2  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1553
Disease ectropion
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:24)
HP:0000501  |  Glaucoma  |  3
HP:0000508  |  Drooping upper eyelid  |  3
HP:0100699  |  Scarring  |  2
HP:0000526  |  Absent iris  |  2
HP:0011498  |  Partial aniridia  |  2
HP:0000968  |  Ectodermal dysplasia  |  1
HP:0000509  |  Conjunctivitis  |  1
HP:0100693  |  Iridodonesis  |  1
HP:0000612  |  Iris coloboma  |  1
HP:0000166  |  Severe periodontal disease  |  1
HP:0002671  |  Basalioma  |  1
HP:0000589  |  Ocular coloboma  |  1
HP:0009926  |  Epiphora  |  1
HP:0000498  |  Inflammation of eyelids  |  1
HP:0000973  |  Dermatomegaly  |  1
HP:0007607  |  Hypohidrotic ectodermal dysplasia  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0001128  |  Trichiasis of eyelid eyelashes  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0000491  |  Corneal inflammation  |  1
HP:0000637  |  Wide palpebral fissure  |  1
HP:0007417  |  Discoid lupus erythematosus  |  1
HP:0007529  |  Hidrotic ectodermal dysplasia  |  1
Disease ID 1553
Disease ectropion
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0152227  |  epiphora  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0013592fluorouracilD00547251-21-8ectropionMESH:D004483marker/mechanism12918558
C0013592tretinoinD014212302-79-4ectropionMESH:D004483marker/mechanism1401316
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)