DiseaseID 3414
背景性视网膜病变
disease
NCI2016_NICHD_1602D:A retinal condition of very immature infants that may be characterized by non-vascularized retina that may lead to neovascularization, scarring, retinal detachment, and blindness.|NCI2016_02D:A bilate
Relationship Network
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Disease: 1Formula: 8Herb: 12Symptom: 6Target: 24Links: 50
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3414
- Core Entity Id
- 59619
- Source Entity Count
- 1
- Preferred Name
- Retinopathy Background
- Name Cn
- 背景性视网膜病变
- Name Pinyin
- Bei Jing Xing Shi Wang Mo Bing Bian
- Name En
- Retinopathy Background
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Eye Diseases; Endocrine System DiseasesEye 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 DiseasesEye Diseases; Endocrine System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_NICHD_1602D:A retinal condition of very immature infants that may be characterized by non-vascularized retina that may lead to neovascularization, scarring, retinal detachment, and blindness.|NCI2016_02D:A bilateral retinopathy characterized by neovascularization, scarring, retinal detachment, and eventually blindness. It may be mild or severe. It occurs in babies born prematurely. Causes include oxygen toxicity and hypoxia.|MSH2017_2016_08_12:A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed)|CSP2006:bilateral retinopathy typically occurring in premature infants treated with high concentrations of oxygen; characterized by vascular dilation, proliferation, and tortuosity, edema, and retinal detachment with ultimate conversion of the retina into a fibrous mass; usually growth of the eye is arrested and may result in microophthalmia; blindness may occur.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Retinopathy Background
Role
preferred
Name
Exudative Vitreoretinopathy 1
Role
preferred
Name
Retinopathy Of Prematurity
Role
preferred
Name
Familial Exudative Vitreoretinopathy
Role
preferred
Name
Nonproliferative Diabetic Retinopathy
Role
preferred
Name
Background Diabetic Retinopathy
Role
alias
Name
CRISWICK-SCHEPENS SYNDROME
Role
alias
Name
EVR1
Role
alias
Name
EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT
Role
alias
Name
Exudative Vitreoretinopathy
Role
alias
Name
Eye And Adnexa Disease
Role
alias
Name
FEVR, AUTOSOMAL DOMINANT
Role
alias
Name
ROP
Role
alias
Name
Retrolental Fibroplasia
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0500049
Herb
HBDIS000292HBDIS000293HBDIS002626HBDIS007754HBDIS016795
Me Sh
D012178
Omim
133780
Umls
C0035344C1851402
Icd10
H35.1
Med Dra
10038933
Sym Map
SMDE01598SMDE03023
Do Class
DOID:630DOID:7
Dis Ge Net
C0004606C0004608C0035344C0339539C1851402
Orphanet
90050
Umls Sty
T019T047
Hpo Class
HP:0000478
Me Sh Class
C11C14C16C19
Etcm Disease
Exudative Vitreoretinopathy 1
Tcmbank Disease
119592021020494309597260
Itcmdb Generated
ITX-DISEASE-72FE742D70D6
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2
Suppress
0
Page Title
Disease Exudative Vitreoretinopathy 1 Details page
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
disease
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 Syndrome
Basic Information
Disease Name
Exudative Vitreoretinopathy 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Cardiovascular diseases;Eye diseases;Neuronal diseases
Disease Definition
NCI2016_NICHD_1602D:A retinal condition of very immature infants that may be characterized by non-vascularized retina that may lead to neovascularization, scarring, retinal detachment, and blindness.|NCI2016_02D:A bilateral retinopathy characterized by neovascularization, scarring, retinal detachment, and eventually blindness. It may be mild or severe. It occurs in babies born prematurely. Causes include oxygen toxicity and hypoxia.|MSH2017_2016_08_12:A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed)|CSP2006:bilateral retinopathy typically occurring in premature infants treated with high concentrations of oxygen; characterized by vascular dilation, proliferation, and tortuosity, edema, and retinal detachment with ultimate conversion of the retina into a fibrous mass; usually growth of the eye is arrested and may result in microophthalmia; blindness may occur.Retinopathy of prematurity (ROP) is a rare retinal vasoproliferative disorder affecting preterm infants characterized initially by a delay in physiologic retinal vascular development, and subsequently
Me Sh Disease Class
Cardiovascular Diseases; Eye Diseases; Endocrine System DiseasesEye 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 DiseasesEye Diseases; Endocrine System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome