DiseaseID 15571
角膜营养不良
disease
MSH2017_2016_08_12:Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macul
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Disease: 1Formula: 17Herb: 12Symptom: 12Target: 24Links: 65
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 15571
- Core Entity Id
- 73521
- Source Entity Count
- 1
- Preferred Name
- Corneal Dystrophy
- Name Cn
- 角膜营养不良
- Name Pinyin
- Jiao Mo Ying Yang Bu Liang
- Name En
- Corneal Dystrophy
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Eye Diseases; Nervous System DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the eye
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesEye Diseases; Nervous System Diseases; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Corneal Dystrophy
Role
preferred
Name
Corneal Dystrophy, Congenital Stromal
Role
preferred
Name
Corneal Dystrophy, Epithelial Basement Membrane
Role
preferred
Name
Corneal Dystrophy, Posterior Polymorphous, 2
Role
preferred
Name
Corneal Dystrophy, Subepithelial Mucinous
Role
preferred
Name
Hereditary Corneal Dystrophy
Role
preferred
Name
CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS
Role
preferred
Name
CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS
Role
preferred
Name
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)
Role
preferred
Name
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT
Role
preferred
Name
Granular Dystrophy, Corneal
Role
preferred
Name
Groenouw'S Dystrophies
Role
preferred
Name
Macular Corneal Dystrophy
Role
preferred
Name
Macular Corneal Dystrophy Type Ii (Disorder)
Role
preferred
Name
Macular Dystrophy, Corneal Type 1
Role
preferred
Name
Polymorphous Corneal Dystrophy
Role
preferred
Name
Stromal Dystrophies, Corneal
Role
preferred
Name
COGAN CORNEAL DYSTROPHY
Role
alias
Name
CONGENITAL STROMAL CORNEAL DYSTROPHY
Role
alias
Name
CORNEAL DYSTROPHY, ANTERIOR BASEMENT MEMBRANE
Role
alias
Name
CORNEAL DYSTROPHY, MAP-DOT-FINGERPRINT TYPE
Role
alias
Name
CORNEAL DYSTROPHY, MICROCYSTIC
Role
alias
Name
CSCD
Role
alias
Name
Corneal Dystrophies, Hereditary
Role
alias
Name
Corneal Dystrophy, Hereditary
Role
alias
Name
Corneal Dystrophy, Posterior Polymorphous, 1
Role
alias
Name
Corneal Dystrophy, Posterior Polymorphous, 3
Role
alias
Name
Corneal Endothelial Dystrophy 1, Autosomal Dominant, Formerly
Role
alias
Name
Corneal Macular Dystrophy
Role
alias
Name
EBMD
Role
alias
Name
Epithelial Basement Membrane Dystrophy
Role
alias
Name
Granular Corneal Dystrophy
Role
alias
Name
Hereditary Corneal Dystrophies
Role
alias
Name
Lisch Epithelial Corneal Dystrophy
Role
alias
Name
Macular Corneal Dystrophy, Type Ii
Role
alias
Name
Macular Dystrophy, Corneal
Role
alias
Name
PPCD2
Role
alias
Name
Polymorphous Posterior Corneal Dystrophy
Role
alias
Name
Posterior Amorphous Corneal Dystrophy
Role
alias
Name
Posterior Polymorphous Corneal Dystrophy
Role
alias
Name
Posterior Polymorphous Corneal Dystrophy 1
Role
alias
Name
Posterior Polymorphous Corneal Dystrophy 2
Role
alias
Name
Posterior Polymorphous Corneal Dystrophy 3
Role
alias
Name
Subepithelial Mucinous Corneal Dystrophy
Role
alias
Name
X-Linked Endothelial Corneal Dystrophy
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001131HP:0007802HP:0007915
Herb
HBDIS000662HBDIS000663HBDIS001215HBDIS001226HBDIS001825HBDIS002856HBDIS007720HBDIS009892HBDIS014679HBDIS014691HBDIS015474HBDIS016889HBDIS017436HBDIS018119HBDIS019758HBDIS019759HBDIS028907
Me Sh
D003317
Omim
121820122000217400217800609140609141610048612867612868
Umls
C0010035C0521723C1852795C1857572C1864738C2748503
Icd10
H18.5H18.50
Sym Map
SMDE00720SMDE02569SMDE02885SMDE03677SMDE07566SMDE09414
Do Class
DOID:630DOID:7
Dis Ge Net
C0010035C0010036C0018179C0018245C0024439C0038457C0339284C0521723C1636149C1691013C1836724C1852555C1852795C1857572C1864738C2748502C2748503
Orphanet
1490
Umls Sty
T047
Hpo Class
HP:0000478
Me Sh Class
C09C10C11C14C16C23
Etcm Disease
Corneal Dystrophy and Perceptive DeafnessCorneal Dystrophy, Congenital StromalCorneal Dystrophy, Epithelial Basement MembraneCorneal Dystrophy, Posterior AmorphousCorneal Dystrophy, Posterior Polymorphous, 2Corneal Dystrophy, Subepithelial Mucinous
Tcmbank Disease
1193316424183201936919420750231192510129843301973045949175050681972308010
Itcmdb Generated
ITX-DISEASE-2BEA0B186C50ITX-DISEASE-9AC619E3AD91ITX-DISEASE-A8A630941F28ITX-DISEASE-A8F1E99F83D2ITX-DISEASE-CF19928CC909ITX-DISEASE-F8CEC8791CF3ITX-DISEASE-F9B9648F81AA
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Corneal Dystrophy and Perceptive Deafness Details pageDisease Corneal Dystrophy, Congenital Stromal Details pageDisease Corneal Dystrophy, Epithelial Basement Membrane Details pageDisease Corneal Dystrophy, Posterior Amorphous Details pageDisease Corneal Dystrophy, Posterior Polymorphous, 2 Details pageDisease Corneal Dystrophy, Subepithelial Mucinous Details page
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
diseasegroup
Hpo Class Name
Abnormality of the eye
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the eye
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Corneal Dystrophy and Perceptive Deafness
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Ear diseases;Eye diseases
Disease Name
Corneal Dystrophy, Congenital Stromal
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Corneal Dystrophy, Epithelial Basement Membrane
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Corneal Dystrophy, Posterior Amorphous
Global Category
Rare diseases
Anatomical Category
Eye diseases
Disease Name
Corneal Dystrophy, Posterior Polymorphous, 2
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Corneal Dystrophy, Subepithelial Mucinous
Global Category
Rare diseases
Anatomical Category
Eye diseases
Disease Definition
MSH2017_2016_08_12:Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
Me Sh Disease Class
Cardiovascular Diseases; Eye Diseases; Nervous System DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesEye Diseases; Nervous System Diseases; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Umls Semantic Type Name
Disease or Syndrome