has characteristic has characteristic has material basis in germline mutation in RS1 X-linked inheritance X-linked disease retinoschisis X-linked retinoschisis https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/retinoschisis_1_x_linked_juvenile XJR juvenile X-linked retinoschisis GARD:0004690 X-linked juvenile retinoschisis 1 NCIT:C75483 OMIM:312700 retinoschisis juvenile X chromosome-linked RS1 MEDGEN:811458 A genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration. MONDO:0010725 RS retinoschisis X-linked Orphanet:792 SCTID:86923008 NANDO:1200938 icd11.foundation:2074506458 DOID:0060763 NORD:1864 X-linked juvenile retinoschisis XLRS1 retinoschisis, X-linked retinoschisis 1, X-linked, juvenile UMLS:C3714753 retinoschisis, X-linked recessive XLRS X-linked juvenile retinoschisis type 1 juvenile retinoschisis X-linked retinoschisis inherited retinal dystrophy vitreoretinal degeneration