DiseaseID 15167
上皮复发性糜烂性营养不良
disease
SNOMEDCT_US_2016_09_01:A rare form of superficial corneal dystrophy with recurrent episodes of epithelial erosions from childhood in the absence of associated diseases. The erosions begin spontaneously or are precipitate
Relationship Network
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Disease: 1Formula: 4Herb: 12Symptom: 3Target: 18Links: 43
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 15167
- Core Entity Id
- 73062
- Source Entity Count
- 1
- Preferred Name
- Epithelial Recurrent Erosion Dystrophy
- Name Cn
- 上皮复发性糜烂性营养不良
- Name Pinyin
- Shang Pi Fu Fa Xing Mi Lan Xing Ying Yang Bu Liang
- Name En
- Epithelial Recurrent Erosion Dystrophy
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:A rare form of superficial corneal dystrophy with recurrent episodes of epithelial erosions from childhood in the absence of associated diseases. The erosions begin spontaneously or are precipitated by minor trauma, dust or smoke. The condition may become apparent by 6 months of age, but as a rule it only starts at 4 to 6 years of age. Most patients have attacks of redness, photophobia, epiphora, and ocular pain. Some experience a burning sensation and report sensitive eyes for years. Vision is sometimes impaired. Autosomal dominant pattern of inheritance.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Epithelial Recurrent Erosion Dystrophy
Role
preferred
Name
CORNEAL EROSIONS, RECURRING HEREDITARY
Role
alias
Name
ERED
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS016888
Omim
122400
Umls
C1852551
Sym Map
SMDE04875
Dis Ge Net
C1852551
Umls Sty
T047
Me Sh Class
C11C16
Etcm Disease
Epithelial Recurrent Erosion Dystrophy
Tcmbank Disease
25575
Itcmdb Generated
ITX-DISEASE-6177B0E91659
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Epithelial Recurrent Erosion Dystrophy Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Epithelial Recurrent Erosion Dystrophy
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Definition
SNOMEDCT_US_2016_09_01:A rare form of superficial corneal dystrophy with recurrent episodes of epithelial erosions from childhood in the absence of associated diseases. The erosions begin spontaneously or are precipitated by minor trauma, dust or smoke. The condition may become apparent by 6 months of age, but as a rule it only starts at 4 to 6 years of age. Most patients have attacks of redness, photophobia, epiphora, and ocular pain. Some experience a burning sensation and report sensitive eyes for years. Vision is sometimes impaired. Autosomal dominant pattern of inheritance.
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Umls Semantic Type Name
Disease or Syndrome