MeSH Browser

MeSH Supplementary: Wieacker syndrome
Unique ID: C536703
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536703
Entry Term(s): Apraxia, oculomotor, with congenital contractures and muscle atrophy; Contractures of feet, muscle atrophy, and oculomotor apraxia; Mental Retardation, X-Linked, with Congenital Contractures and Low Fingertip Arches; Mental retardation, X-linked, syndromic 4; Miles-Carpenter x-linked mental retardation syndrome; Wieacker Wolff syndrome; Wieacker-Wolff Syndrome
Registry Numbers: 0
Heading Mapped to: *Apraxias; *Contracture; *Muscular Atrophy; *Ophthalmoplegia; *Genetic Diseases, X-Linked
Frequency: 7
Date of Entry: 2010/08/25
Revision Date: 2023/04/27

Wieacker syndrome MeSH Supplementary Concept Data 2025