ITCMDBv1
DiseaseID 4740

视物显小症

disease

#8805;-10.00 D)), nystagmus, strabismus, normal color vision and fundus abnormalities.

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Disease: 1Symptom: 8Target: 24Links: 32
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Record Fields

Scalar fields from the final disease record.

Disease Id
4740
Core Entity Id
61134
Source Entity Count
1
Preferred Name
Micropsia
Name Cn
视物显小症
Name Pinyin
Shi Wu Xian Xiao Zheng
Name En
Micropsia
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Disgenet Type
disease
Mesh Class
Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesEye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
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 DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Hpo Class Name
Abnormality of the eye
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Definition
#8805;-10.00 D)), nystagmus, strabismus, normal color vision and fundus abnormalities.
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Micropsia
Role
preferred
Name
Cone-Rod Synaptic Disorder, Congenital Nonprogressive
Role
preferred
Name
Csnb, Incomplete, Autosomal Recessive
Role
preferred
Name
Night Blindness
Role
preferred
Name
Night Blindness, Congenital Stationary, Autosomal Dominant 2
Role
preferred
Name
Night Blindness, Congenital Stationary, Autosomal Dominant 3
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 1A
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 1B
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 1C
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 1D
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 2A
Role
preferred
Name
Oguchi Disease 1
Role
preferred
Name
Complete Congenital Stationary Night Blindness
Role
preferred
Name
Congenital Stationary Night Blindness
Role
preferred
Name
Hemeralopia
Role
preferred
Name
Low Vision
Role
preferred
Name
Macropsia
Role
preferred
Name
Metamorphopsia
Role
preferred
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H
Role
preferred
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
Role
preferred
Name
Night Blindness, Congenital Stationary
Role
preferred
Name
Night Blindness, Congenital Stationary, Type 1
Role
preferred
Name
Night Blindness, Stationary
Role
preferred
Name
Nyctalopia
Role
preferred
Name
Oguchi Disease
Role
preferred
Name
Vision Disability
Role
preferred
Name
Vision Disorders
Role
preferred
Name
Visual Impairment
Role
preferred
Name
X-Linked Csnb
Role
preferred
Name
CRSD
Role
alias
Name
CSNB, COMPLETE, AUTOSOMAL RECESSIVE
Role
alias
Name
CSNB, COMPLETE, X-LINKED
Role
alias
Name
CSNB, INCOMPLETE, X-LINKED
Role
alias
Name
CSNB1A
Role
alias
Name
CSNB1B
Role
alias
Name
CSNB1C
Role
alias
Name
CSNB1D
Role
alias
Name
CSNB2
Role
alias
Name
CSNB2A
Role
alias
Name
CSNB2B, FORMERLY
Role
alias
Name
CSNBAD2
Role
alias
Name
CSNBAD3
Role
alias
Name
CSNBO1
Role
alias
Name
Congenital Night Blindness
Role
alias
Name
Congenital Stationary Night Blindness 1A
Role
alias
Name
Congenital Stationary Night Blindness 1B
Role
alias
Name
Congenital Stationary Night Blindness 1C
Role
alias
Name
Congenital Stationary Night Blindness 1D
Role
alias
Name
Congenital Stationary Night Blindness 1H
Role
alias
Name
Congenital Stationary Night Blindness 2A
Role
alias
Name
Congenital Stationary Night Blindness Autosomal Dominant 2
Role
alias
Name
Congenital Stationary Night Blindness Autosomal Dominant 3
Role
alias
Name
Day Blindness
Role
alias
Name
HEMERALOPIA-MYOPIA
Role
alias
Name
Hereditary Night Blindness
Role
alias
Name
Impaired Vision
Role
alias
Name
Loss of Eyesight
Role
alias
Name
MYOPIA-NIGHT BLINDNESS
Role
alias
Name
NBM1
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE, FORMERLY
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, NOUGARET TYPE
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 1
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, RAMBUSCH TYPE
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY
Role
alias
Name
NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA
Role
alias
Name
Night Blindness Since Birth
Role
alias
Name
Night Blindness, Congenital
Role
alias
Name
Night Blindness, Congenital Stationary, Complete
Role
alias
Name
Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive
Role
alias
Name
Oguchi Disease-1
Role
alias
Name
Poor Night Vision
Role
alias
Name
Poor Vision
Role
alias
Name
Static Congenital Hemeralopia
Role
alias
Name
Vision, Low
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0007642HP:0012047HP:0012508HP:0030640
Herb
HBDIS001297HBDIS002135HBDIS003114HBDIS003115HBDIS004823HBDIS004824HBDIS006569HBDIS007752HBDIS013428HBDIS016439HBDIS016703HBDIS018147HBDIS018513HBDIS019883HBDIS020783HBDIS021444HBDIS021514HBDIS021551HBDIS021711HBDIS021945HBDIS022075HBDIS025280HBDIS025317HBDIS026319HBDIS027311HBDIS029026
Omim
163500257270258100300071610427610444613216613830617024
Umls
C1306122C1848172C1850362C1864870C1864877C1876182C2750747C3151193C3495587C4041558
Icd10
H53.63
Sym Map
SMDE01327SMDE01978SMDE01979SMDE02349SMDE02589SMDE03384SMDE03774SMDE03881SMDE04472SMDE04487SMDE07660SMDE11489
Do Class
DOID:630DOID:7
Dis Ge Net
C0018975C0028077C0042790C0042798C0233769C0233771C0271185C0339535C1306122C1848172C1850362C1864870C1864877C1876182C2750747C3151193C3489704C3495587C3501847C3551052C3665347C3711543C4041558C4048798C4310758C4551824
Orphanet
215
Umls Sty
T019T033T047T184
Hpo Class
HP:0000478
Me Sh Class
C10C11C16C23
Etcm Disease
Cone-Rod Synaptic Disorder, Congenital NonprogressiveCongenital Stationary Night Blindness
Tcmbank Disease
14844167581718518001888188801914619186196941976519843208921358218862213023036239582422925740271302877929775480574971407272919692819919
Itcmdb Generated
ITX-DISEASE-167FA20DA40EITX-DISEASE-28F8552EF24CITX-DISEASE-3A403F06ED49ITX-DISEASE-716E2EAB331CITX-DISEASE-78FB7E71F35AITX-DISEASE-7C25A81D7BD6ITX-DISEASE-7F1A3C0BA96BITX-DISEASE-98BB5E7890A6

Attributes

Merged source attributes and domain-specific metadata.

Version
v1v1,v2v2
Suppress
0
Page Title
Disease Cone-Rod Synaptic Disorder, Congenital Nonprogressive Details pageDisease Congenital Stationary Night Blindness Details page
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
diseasegroupphenotype
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
Congenital AbnormalityDisease or SyndromeFindingSign or Symptom
Basic Information
Disease Name
Cone-Rod Synaptic Disorder, Congenital Nonprogressive
Global Category
Genetic diseases
Anatomical Category
Eye diseases
Disease Name
Congenital Stationary Night Blindness
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Mental diseases
Disease Definition
#8805;-10.00 D)), nystagmus, strabismus, normal color vision and fundus abnormalities.NCI2016_NICHD_1602D:Poor visual function in dim light.|NCI2016_CTCAE_1602D:A disorder characterized by an inability to see clearly in dim light.|NCI2016_02D:Inability to see clearly in dim light.|NCI2016_02D:An inability to see clearly in dim light; due to a deficiency of vitamin A or to a retinal disorder.|MSH2017_2016_08_12:Failure or imperfection of vision at night or in dim light, with good vision only on bright days. (Dorland, 27th ed)|HPO2016_07_04:Inability to see well at night or in poor light. [HPO:probinson]|CSP2006:failure or imperfection of vision at night or in dim light, with good vision only on bright days.
Me Sh Disease Class
Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesEye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasegroupphenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesEye DiseasesPathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or SyndromeFindingSign or Symptom