DiseaseID 2493
先天性眼球震颤
disease
MSH2017_2016_08_12:Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 2Target: 12Links: 14
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2493
- Core Entity Id
- 2819
- Source Entity Count
- 1
- Preferred Name
- Congenital Nystagmus
- Name Cn
- 先天性眼球震颤
- Name Pinyin
- Xian Tian Xing Yan Qiu Zhen Chan
- Name En
- Congenital Nystagmus
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the eye
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)|HPO2016_07_04:Nystagmus dating from or present at birth. [HPO:curators]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Congenital Nystagmus
Role
preferred
Name
Nystagmus 6, Congenital, X-Linked
Role
preferred
Name
NYS6
Role
alias
Name
Nystagmus, Congenital
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0006934
Herb
HBDIS010691HBDIS029293
Me Sh
D020417
Omim
300814
Umls
C0700501C3151752
Icd10
H55.01
Sym Map
SMDE01548SMDE07479
Do Class
DOID:7
Dis Ge Net
C0700501C3151752
Umls Sty
T019T047
Hpo Class
HP:0000478
Me Sh Class
C10C11C16
Tcmbank Disease
4666
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
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
Congenital AbnormalityDisease or Syndrome
Disease Definition
MSH2017_2016_08_12:Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)|HPO2016_07_04:Nystagmus dating from or present at birth. [HPO:curators]
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Umls Semantic Type Name
Congenital Abnormality