MeSH Browser

MeSH Supplementary: Myopathy, congenital nonprogressive with Moebius and Robin sequences
Unique ID: C536102
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536102
Entry Term(s): Carey Fineman Ziter syndrome; Carey-Fineman-Ziter Syndrome; Congenital nonprogressive myopathy with Moebius and Robin sequence; Moebius sequence, Robin complex, and hypotonia; Myopathy, Congenital Nonprogressive, with Moebius Sequence and Robin Sequence
Registry Number: 0
Heading Mapped to: *Muscular Diseases; *Pierre Robin Syndrome; *Mobius Syndrome
Frequency: 9
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Myopathy, congenital nonprogressive with Moebius and Robin sequences MeSH Supplementary Concept Data 2024