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Diseases

Retinoschisis

retinoschisis

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]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
04
PHEX
phosphate regulating endopeptidase homolog X-linked
phosphate regulating endopeptidase homolog X-linked
07
RPE
ribulose-5-phosphate-3-epimerase
ribulose-5-phosphate-3-epimerase