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X-Linked Retinoschisis (MONDO:0010725)

A genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration.

Overview

Category

Ontology ID

Internal:11865

Synonyms

X-linked juvenile retinoschisis

X-linked juvenile retinoschisis type 1

X-linked retinoschisis

XLRS

juvenile X-linked retinoschisis

retinoschisis, X-linked

retinoschisis, X-linked recessive

RS1

X-linked juvenile retinoschisis 1

XJR

XLRS1

juvenile retinoschisis

retinoschisis 1, X-linked, juvenile

retinoschisis X-linked

retinoschisis juvenile X chromosome-linked

Mapped terms

DOID:0060763

GARD:0004690

MEDGEN:811458

NANDO:1200938

NCIT:C75483

NORD:1864

OMIM:312700

Orphanet:792

SCTID:86923008

UMLS:C3714753

icd11.foundation:2074506458

Child terms

Unknown children.