DiseaseID 2608
近视
disease
NCI2016_02D:The condition in which the individual does not see far distances clearly.|MSH2017_2016_08_12:A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in fro
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 7Symptom: 12Target: 24Links: 43
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2608
- Core Entity Id
- 2955
- Source Entity Count
- 1
- Preferred Name
- Myopia
- Name Cn
- 近视
- Name Pinyin
- Jin Shi
- Name En
- Myopia
- 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
- Abnormality of the eye
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesEye Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:The condition in which the individual does not see far distances clearly.|MSH2017_2016_08_12:A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness.|HPO2016_07_04:An abnormality of refraction characterized by the ability to see objects nearby clearly, while objects in the distance appear blurry. [HPO:probinson]|CSP2006:a refractive error in which rays of light entering the eye parallel to the optic axis are brought to a focus in front of the retina, as a result of the eyeball being too long from front to back; also called nearsightedness because the near point is less distant than it is in emmetropia with an equal amplitude of accommodation.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Myopia
Role
preferred
Name
Myopia 21, Autosomal Dominant
Role
preferred
Name
Myopia 22, Autosomal Dominant
Role
preferred
Name
Myopia 23, Autosomal Recessive
Role
preferred
Name
Myopia 24, Autosomal Dominant
Role
preferred
Name
MYOPIA 1, X-LINKED
Role
preferred
Name
MYOPIA 2 (disorder)
Role
preferred
Name
MYOPIA 3 (disorder)
Role
preferred
Name
MYOPIA 6 (disorder)
Role
preferred
Name
Myopia, Susceptibility To
Role
preferred
Name
Close Sighted
Role
alias
Name
MYP21
Role
alias
Name
MYP22
Role
alias
Name
MYP23
Role
alias
Name
MYP24
Role
alias
Name
Myopia 1
Role
alias
Name
Myopia 2
Role
alias
Name
Myopia 2, Autosomal Dominant
Role
alias
Name
Myopia 3
Role
alias
Name
Myopia 3, Autosomal Dominant
Role
alias
Name
Myopia 6
Role
alias
Name
Myopia, X-Linked
Role
alias
Name
Myp2
Role
alias
Name
Myp3
Role
alias
Name
Near Sighted
Role
alias
Name
Near Sightedness
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000545
Herb
HBDIS002035HBDIS015249HBDIS015530HBDIS015773HBDIS018077HBDIS020224HBDIS021251HBDIS023061HBDIS029483HBDIS029484
Me Sh
D009216
Omim
608908614167615420615431615946
Umls
C0027092C3279997C3809464C3809482C4014762
Icd10
H52.1
Sym Map
SMDE02444SMDE02722SMDE03960SMDE04970SMDE11256
Do Class
DOID:7
Dis Ge Net
C0027092C1834531C1837148C1839612C1864111C2931111C3279997C3809464C3809482C4014762
Umls Sty
T047
Hpo Class
HP:0000478
Me Sh Class
C11C16
Etcm Disease
Myopia 21, Autosomal DominantMyopia 22, Autosomal DominantMyopia 23, Autosomal RecessiveMyopia 24, Autosomal Dominant
Tcmbank Disease
101261115115832210623659297529871308231398
Itcmdb Generated
ITX-DISEASE-1EB7E15CC63BITX-DISEASE-3B63D1FF9034ITX-DISEASE-CFC7ADB8B9ADITX-DISEASE-E376FCBD9B75ITX-DISEASE-FA1C501D946C
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Myopia 21, Autosomal Dominant Details pageDisease Myopia 22, Autosomal Dominant Details pageDisease Myopia 23, Autosomal Recessive Details pageDisease Myopia 24, Autosomal Dominant Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the eye
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the eye
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Myopia 21, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Myopia 22, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Myopia 23, Autosomal Recessive
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Name
Myopia 24, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Disease Definition
NCI2016_02D:The condition in which the individual does not see far distances clearly.|MSH2017_2016_08_12:A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness.|HPO2016_07_04:An abnormality of refraction characterized by the ability to see objects nearby clearly, while objects in the distance appear blurry. [HPO:probinson]|CSP2006:a refractive error in which rays of light entering the eye parallel to the optic axis are brought to a focus in front of the retina, as a result of the eyeball being too long from front to back; also called nearsightedness because the near point is less distant than it is in emmetropia with an equal amplitude of accommodation.
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