01
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Retinoschisis
- Standard Disease Name
- retinoschisis
- MeSH Tree
- No data
- ICD-10
- H33.10
Identifiers
- DO ID
- No data
- MeSH ID
- D041441
- OMIM ID
- MTHU006950
- UMLS ID
- C0152439
- HPO ID
- No data
Description and Extensions
- Description
- 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]
