X-linked juvenile retinoschisis 1

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Summary

Literature (0)

DOID:0060763 - X-linked juvenile retinoschisis 1

Disease Ontology Definition:A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that has_material_basis_in the RS1 gene on chromosome Xp22.

Synonyms: X-linked juvenile retinoschisis, X-linked retinoschisis, XLRS

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:312700 - retinoschisis 1, x-linked, juvenile; rs1

MIM:312700 - retinoschisis 1, x-linked, juvenile; rs1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): retinoschisis (is_a), X-linked recessive disease (is_a)