DiseaseID 2074
视网膜劈裂症
disease
NCI2016_02D:An inherited or acquired disorder characterized by splitting of the retina into two layers. It results in loss of vision.|MSH2017_2016_08_12:A vitreoretinal dystrophy characterized by splitting of the neurore
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Experiment: 1Symptom: 3Target: 12Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2074
- Core Entity Id
- 2333
- Source Entity Count
- 1
- Preferred Name
- Retinoschisis
- Name Cn
- 视网膜劈裂症
- Name Pinyin
- Shi Wang Mo Pi Lie Zheng
- Name En
- Retinoschisis
- 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; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the eye
- Mesh Class Name
- Eye Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_02D:An inherited or acquired disorder characterized by splitting of the retina into two layers. It results in loss of vision.|MSH2017_2016_08_12:A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome-linked juvenile retinoschisis.|HPO2016_07_04:Splitting of the neuroretinal layers of the retina. [HPO:probinson]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Retinoschisis
Role
preferred
Name
Retinoschisis 1, X-Linked, Juvenile
Role
preferred
Name
X-Linked Retinoschisis
Role
preferred
Name
Congenital Anomaly of Retina
Role
preferred
Name
Congenital Retinal Aneurysm
Role
preferred
Name
Retinoschisis, Degenerative
Role
preferred
Name
Retinoschisis, Juvenile, X-Linked
Role
preferred
Name
Congenital Malformation of Retina
Role
alias
Name
RS
Role
alias
Name
RS1
Role
alias
Name
X-Linked Juvenile Retinoschisis 1
Role
alias
Name
X-linked Juvenile Retinoschisis
Role
alias
Name
XLRS
Role
alias
Name
XLRS1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0030502
Herb
HBDIS003727HBDIS006558HBDIS022111HBDIS028360HBDIS028361HBDIS028637
Me Sh
D041441
Omim
312700
Umls
C0152439C0271091C3714753
Icd10
H33.10Q14.1
Sym Map
SMDE02186SMDE03923SMDE12850
Do Class
DOID:630DOID:7
Dis Ge Net
C0152439C0266564C0266571C0271091C1137478C3714753
Orphanet
792
Umls Sty
T019T047
Hpo Class
HP:0000478
Me Sh Class
C04C11C16
Tcmbank Disease
18427205624713
Itcmdb Generated
ITX-DISEASE-5A9A3319FD4F
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
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
Disease Definition
NCI2016_02D:An inherited or acquired disorder characterized by splitting of the retina into two layers. It results in loss of vision.|MSH2017_2016_08_12:A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome-linked juvenile retinoschisis.|HPO2016_07_04:Splitting of the neuroretinal layers of the retina. [HPO:probinson]X-linked retinoschisis (XLRS) is a genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration.
Me Sh Disease Class
Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Eye Diseases
Umls Semantic Type Name
Disease or Syndrome