MeSH Browser

MeSH Supplementary: Grubben de Cock Borghgraef syndrome
Unique ID: C537621
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537621
Registry Numbers: 0
Heading Mapped to: *Developmental Disabilities; Eczema / congenital; Muscle Hypotonia / congenital; *Tooth Abnormalities; *Limb Deformities, Congenital
Frequency: 0
Note: Severe growth retardation, developmental delay with hypotonia, hypotrophy of the distal extremities, dental anomalies, and eczematous skin
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Grubben de Cock Borghgraef syndrome MeSH Supplementary Concept Data 2025