- Concept UI
- M0430675
- Scope Note
- X chromosome recessive disorder, found nearly exclusively in males and becoming apparent around puberty. Characterized initially by a cystlike structure involving the FOVEA CENTRALIS, a peripheral retinoschisis occurs in about half the patients.
- Terms
-
Retinoschisis, Juvenile, X-Linked
Preferred Term
Term UI
T503756
Date07/12/2002
LexicalTag
NON
ThesaurusID
-
Retinoschisis, Juvenile, X Chromosome-Linked
Term UI
T503764
Date07/12/2002
LexicalTag
NON
ThesaurusID
NLM (2003)
-
X-Linked Juvenile Retinoschisis
Term UI
T768280
Date03/31/2010
LexicalTag
NON
ThesaurusID
-
Retinoschisis X-Linked Juvenile
Term UI
T768281
Date03/31/2010
LexicalTag
NON
ThesaurusID
-
Congenital X-Linked Retinoschisis
Term UI
T842755
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Retinoschisis, X-Linked
Term UI
T503757
Date07/12/2002
LexicalTag
NON
ThesaurusID
NLM (2003)
-
X-Linked Retinoschisis
Term UI
T503759
Date07/12/2002
LexicalTag
NON
ThesaurusID
-
Retinoschisis, Juvenile
Term UI
T503758
Date07/12/2002
LexicalTag
NON
ThesaurusID
NLM (2003)