DiseaseID 4045
钱德勒综合征
disease
NCI2016_02D:An autosomal dominant, bilateral, slowly progressive degeneration of corneal endothelial cells with thickening of Descemet's membrane and accumulation of excrescences. It results in corneal edema and loss of
Relationship Network
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Disease: 1Formula: 17Herb: 12Symptom: 1Target: 24Links: 54
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4045
- Core Entity Id
- 60332
- Source Entity Count
- 1
- Preferred Name
- Chandler Syndrome
- Name Cn
- 钱德勒综合征
- Name Pinyin
- Qian De Lei Zong He Zheng
- Name En
- Chandler Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesEye Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:An autosomal dominant, bilateral, slowly progressive degeneration of corneal endothelial cells with thickening of Descemet's membrane and accumulation of excrescences. It results in corneal edema and loss of vision.|MSH2017_2016_08_12:Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.|CSP2006:disorder caused by loss of endothelium of the central cornea; it is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Chandler Syndrome
Role
preferred
Name
Corneal Dystrophy, Fuchs Endothelial, 1
Role
preferred
Name
Corneal Dystrophy, Fuchs Endothelial, 2
Role
preferred
Name
Corneal Dystrophy, Fuchs Endothelial, 4
Role
preferred
Name
Corneal Dystrophy, Fuchs Endothelial, 6
Role
preferred
Name
Corneal Dystrophy, Fuchs Endothelial, 8
Role
preferred
Name
Fuchs Endothelial Dystrophy
Role
preferred
Name
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3
Role
preferred
Name
Corneal Dystrophy, Fuchs' Endothelial, 1
Role
preferred
Name
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, EARLY-ONSET
Role
alias
Name
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET
Role
alias
Name
Corneal Dystrophy, Fuchs' Endothelial, 2
Role
alias
Name
FECD1
Role
alias
Name
FECD4
Role
alias
Name
FECD6
Role
alias
Name
FECD8
Role
alias
Name
Fuchs' Endothelial Corneal Dystrophy 2
Role
alias
Name
Fuchs' Endothelial Dystrophy
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001114HBDIS010048HBDIS016766HBDIS017480HBDIS019859HBDIS019860HBDIS019861HBDIS022375
Me Sh
D005642D057129
Omim
136800613268613270615523
Umls
C0016781C1850959C1857800C2750448C2750450C3809798
Icd10
H18.51
Sym Map
SMDE02225SMDE02818SMDE03535SMDE04654SMDE07565SMDE08868
Do Class
DOID:7
Dis Ge Net
C0016781C0544008C1850959C1857800C2750448C2750450C2750451C3809798
Umls Sty
T047
Me Sh Class
C11C16
Etcm Disease
Corneal Dystrophy, Fuchs Endothelial, 1Corneal Dystrophy, Fuchs Endothelial, 2Corneal Dystrophy, Fuchs Endothelial, 3Corneal Dystrophy, Fuchs Endothelial, 4Corneal Dystrophy, Fuchs Endothelial, 6Corneal Dystrophy, Fuchs Endothelial, 8
Tcmbank Disease
10324108091376517923193851979440088102
Itcmdb Generated
ITX-DISEASE-444686F4CA85ITX-DISEASE-73B4813263DDITX-DISEASE-7AB71927F50AITX-DISEASE-7DFFFE3FEE3BITX-DISEASE-B4E83CB58541ITX-DISEASE-EFE636E277EE
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Corneal Dystrophy, Fuchs Endothelial, 1 Details pageDisease Corneal Dystrophy, Fuchs Endothelial, 2 Details pageDisease Corneal Dystrophy, Fuchs Endothelial, 3 Details pageDisease Corneal Dystrophy, Fuchs Endothelial, 4 Details pageDisease Corneal Dystrophy, Fuchs Endothelial, 6 Details pageDisease Corneal Dystrophy, Fuchs Endothelial, 8 Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 1
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 2
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 3
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 4
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 6
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Name
Corneal Dystrophy, Fuchs Endothelial, 8
Global Category
Genetic diseases
Anatomical Category
Eye diseases;Gastrointestinal Diseases
Disease Definition
NCI2016_02D:An autosomal dominant, bilateral, slowly progressive degeneration of corneal endothelial cells with thickening of Descemet's membrane and accumulation of excrescences. It results in corneal edema and loss of vision.|MSH2017_2016_08_12:Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.|CSP2006:disorder caused by loss of endothelium of the central cornea; it is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.
Me Sh Disease Class
Eye DiseasesEye 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 DiseasesEye Diseases
Umls Semantic Type Name
Disease or Syndrome