MeSH Browser

MeSH Supplementary: Cerebrocostomandibular Syndrome
Unique ID: C562538
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562538
Entry Term(s): CCM Syndrome; Cerebrocostomandibular-Like Syndrome; Rib Gap Defects with Micrognathia
Registry Number: 0
Heading Mapped to: *Intellectual Disability; *Micrognathism; Ribs / *abnormalities
Frequency: 11
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Cerebrocostomandibular Syndrome MeSH Supplementary Concept Data 2024