DiseaseID 7742
动眼神经失用症
disease
MSH2017_2016_08_12:A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis.
Relationship Network
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Disease: 1Symptom: 5Target: 12Links: 17
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7742
- Core Entity Id
- 64589
- Source Entity Count
- 1
- Preferred Name
- Oculomotor Apraxia
- Name Cn
- 动眼神经失用症
- Name Pinyin
- Dong Yan Shen Jing Shi Yong Zheng
- Name En
- Oculomotor Apraxia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Eye Diseases; Nervous System DiseasesCardiovascular Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the eye; Abnormality of the nervous system
- Mesh Class Name
- Eye Diseases; Nervous System Diseases; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the nervous system; Abnormality of the eye
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Oculomotor Apraxia
Role
preferred
Name
Oculovestibuloauditory Syndrome
Role
preferred
Name
Apraxia, Oculomotor, Cogan Type
Role
preferred
Name
Cogan Syndrome
Role
alias
Name
Diffuse Interstitial Keratitis
Role
alias
Name
Ocular Motor Apraxia
Role
alias
Name
Oculomotor Apraxia, Cogan Type
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000657
Herb
HBDIS006577HBDIS010041HBDIS021450
Me Sh
D055952
Umls
C0271270
Icd10
H16.32
Sym Map
SMDE11585
Do Class
DOID:7
Dis Ge Net
C0271270C0543874C3489733
Umls Sty
T019T047
Hpo Class
HP:0000478HP:0000707
Me Sh Class
C10C11C14C23F01
Tcmbank Disease
10939246863287
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the nervous system; Abnormality of the eye
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the eye; Abnormality of the nervous system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Disease Definition
MSH2017_2016_08_12:A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis.
Me Sh Disease Class
Cardiovascular Diseases; Eye Diseases; Nervous System DiseasesCardiovascular Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Eye Diseases; Nervous System Diseases; Cardiovascular DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome